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WO2024235463A1 - Indénonaphtopyranes ayant un sulfure d'aryle/hétéroaryle à substitution perfluoroalkyle en position-11 - Google Patents

Indénonaphtopyranes ayant un sulfure d'aryle/hétéroaryle à substitution perfluoroalkyle en position-11 Download PDF

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WO2024235463A1
WO2024235463A1 PCT/EP2023/063277 EP2023063277W WO2024235463A1 WO 2024235463 A1 WO2024235463 A1 WO 2024235463A1 EP 2023063277 W EP2023063277 W EP 2023063277W WO 2024235463 A1 WO2024235463 A1 WO 2024235463A1
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substituted
unsubstituted
branched
linear
formula
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Chien-Yang Chiu
Beon-Kyu Kim
Robert W. Walters
Wenjing Xiao
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Transitions Optical Ltd
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Transitions Optical Ltd
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Priority to AU2023448383A priority patent/AU2023448383A1/en
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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B11/00—Diaryl- or thriarylmethane dyes
    • C09B11/02—Diaryl- or thriarylmethane dyes derived from diarylmethanes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00—Other synthetic dyes of known constitution

Definitions

  • the present invention relates to indenonaphthopyran compounds that have a perfluoroalkyl substituted aryl or perfluoroalkyl substituted heteroaryl group bonded to position- 11 by a sulfide linkage, and photochromic compositions and photochromic articles that include such compounds.
  • photochromic compounds In response to certain wavelengths of electromagnetic radiation (or “actinic radiation”), photochromic compounds, such as indenonaphthopyrans (or indeno-fused naphthopyrans), typically undergo a transformation from one form or state to another form, with each form having a characteristic or distinguishable absorption spectrum associated therewith.
  • actinic radiation typically, upon exposure to actinic radiation, many photochromic compounds are transformed from a closed-form, which corresponds to an unactivated (or bleached, e.g., substantially colorless) state of the photochromic compound, to an open-form, which corresponds to an activated (or colored) state of the photochromic compound.
  • compositions and articles, such as eyewear lenses, that contain photochromic compounds or have photochromic compounds applied thereto typically display colorless (e.g., clear) and colored states that correspond to the colorless and colored states of the photochromic compounds contained therein or applied thereto.
  • photochromic indenonaphthopyran compounds provide a significant level of darkness when exposed to actinic radiation. It is also generally desirable that photochromic indenonaphthopyran compounds also quickly fade to the unactivated (or bleached) state in the absence of exposure to actinic radiation. Indenonaphthopyran compounds that provide such a combination of a significant or high level of darkness when exposed to actinic radiation, and a fast fade rate in the absence of actinic radiation, typically and undesirably have a bleached state (or color) that is too dark, and/or poor fatigue resistance.
  • R 4 and R 5 are each independently selected from: substituted or unsubstituted alkyl; or R 4 and R 5 together form a substituted or unsubstituted spirocyclic ring.
  • R 6 independently for each n, and R 7 independently for each m, in each case are independently selected from: amino; substituted or unsubstituted nitrogen-containing heterocycle; a halo group; substituted or unsubstituted alkyl; substituted or unsubstituted alkoxy; perfluoroalkyl; or substituted or unsubstituted alkylthio.
  • a photochromic composition comprising the indenonaphthopyran compound of the present invention.
  • a photochromic article that comprises the indenonaphthopyran compound of the present invention.
  • left-to-right representations of linking groups are inclusive of other appropriate orientations, such as, but not limited to, right-to-left orientations.
  • the left-to-right representation of the divalent linking group representation thereof or equivalently -O(O)C- or -OC(O)-.
  • polymer means homopolymers (e.g., prepared from a single monomer species), copolymers (e.g., prepared from at least two monomer species), and graft polymers.
  • (meth)acrylate and similar terms, such as “(meth)acrylic acid ester” means methacrylates and/or acrylates.
  • (meth)acrylic acid means methacrylic acid and/or acrylic acid.
  • the indenonaphthopyran compounds of the present invention are also referred to herein as photochromic indenonaphthopyran compounds and/or photochromic indenonaphthopyrans.
  • indenonaphthopyran compounds of the present invention can optionally further include one or more coproducts, resulting from the synthesis of such compounds.
  • photochromic and similar terms, such as “photochromic compound” means having an absorption spectrum for at least visible radiation that varies in response to absorption of at least actinic radiation.
  • photochromic material means any substance that is adapted to display photochromic properties (such as, adapted to have an absorption spectrum for at least visible radiation that varies in response to absorption of at least actinic radiation) and which includes at least one photochromic compound.
  • actinic radiation means electromagnetic radiation that is capable of causing a response in a material, such as, but not limited to, transforming a photochromic material from one form or state to another as will be discussed in further detail herein.
  • photochromic material includes thermally reversible photochromic materials and compounds and non-thermally reversible photochromic materials and compounds.
  • thermally reversible photochromic compounds/materials as used herein means compounds/materials capable of converting from a first state, for example a “clear state,” to a second state, for example a “colored state,” in response to actinic radiation, and reverting back to the first state in response to thermal energy.
  • non-thermally reversible photochromic compounds/materials means compounds/materials capable of converting from a first state, for example a “clear state,” to a second state, for example a “colored state,” in response to actinic radiation, and reverting back to the first state in response to actinic radiation of substantially the same wavelength(s) as the absorption(s) of the colored state (e.g., discontinuing exposure to such actinic radiation).
  • the terms “first” and “second” are not intended to refer to any particular order or chronology, but instead refer to two different conditions or properties.
  • the first state and the second state of a photochromic compound can differ with respect to at least one optical property, such as but not limited to the absorption of visible and/or UV radiation.
  • the photochromic compounds of the present invention can have a different absorption spectrum in each of the first and second state.
  • a photochromic compound of the present invention can be clear in the first state and colored in the second state.
  • a photochromic compound of the present invention can have a first color in the first state and a second color in the second state.
  • optical article or element or device means pertaining to or associated with light and/or vision.
  • the optical article or element or device can be chosen from ophthalmic articles, elements and devices, display articles, elements and devices, windows, mirrors, and active and passive liquid crystal cell articles, elements and devices.
  • ophthalmic means pertaining to or associated with the eye and vision.
  • ophthalmic articles or elements include corrective and non-corrective lenses, including single vision or multi-vision lenses, which can be either segmented or non-segmented multi-vision lenses (such as, but not limited to, bifocal lenses, trifocal lenses and progressive lenses), as well as other elements used to correct, protect, or enhance (cosmetically or otherwise) vision, including without limitation, contact lenses, intra-ocular lenses, magnifying lenses, and protective lenses or visors.
  • display means the visible or machine-readable representation of information in words, numbers, symbols, designs or drawings.
  • Non-limiting examples of display elements include screens, monitors, and security elements, such as security marks.
  • window means an aperture adapted to permit the transmission of radiation there-through.
  • windows include automotive and aircraft transparencies, windshields, filters, shutters, and optical switches.
  • mirror means a surface that specularly reflects a large fraction of incident light.
  • liquid crystal cell refers to a structure containing a liquid crystal material that is capable of being ordered.
  • a non-limiting example of a liquid crystal cell element is a liquid crystal display.
  • Ring Position and similar terms, such as “Position-X” or “position-X” means a particular position in the ring structure, such as the fused ring structure, of a chemical compound, such as the indenonaphthopyran compounds of the present invention, and which are depicted herein in accordance with some embodiments by numbers within the ring structures of representative chemical formulas, such as Formula (I).
  • All documents, such as but not limited to issued patents and patent applications, referred to herein, and unless otherwise indicated, are to be considered to be "incorporated by reference” in their entirety.
  • linear or branched groups such as linear or branched alkyl
  • linear or branched alkyl are herein understood to include: a methylene group or a methyl group; groups that are linear, such as linear C2-C20 alkyl groups; and groups that are appropriately branched, such as branched C3-C20 alkyl groups.
  • alkyl as used herein means linear or branched C1-C25 alkyl.
  • Linear or branched alkyl can include C1-C25 alkyl, such as C1-C20 alkyl, such as C2-C10 alkyl, such as C1-C12 alkyl, such as Ci-Ce alkyl.
  • alkyl groups from which the various alkyl groups of the present invention can be selected from include, but are not limited to, those recited further herein.
  • cycloalkyl as used herein means groups that are appropriately cyclic, such as, but not limited to, C3-C12 cycloalkyl (including, but not limited to, cyclic C3-C10 alkyl, or cyclic C5-C7 alkyl) groups. Examples of cycloalkyl groups include, but are not limited to, those recited further herein.
  • cycloalkyl as used herein also includes: bridged ring polycycloalkyl groups (or bridged ring polycyclic alkyl groups), such as, but not limited to, bicyclo[2.2.1]heptyl (or norbomyl) and bicyclo[2.2.2]octyl; and fused ring polycycloalkyl groups (or fused ring polycyclic alkyl groups), such as, but not limited to, octahydro- IH-indenyl, and decahydronaphthalenyl.
  • bridged ring polycycloalkyl groups or bridged ring polycyclic alkyl groups
  • fused ring polycycloalkyl groups or fused ring polycyclic alkyl groups
  • heterocycloalkyl as used herein means groups that are appropriately cyclic, such as, but not limited to, C2-C12 heterocycloalkyl groups, such as C2-C10 heterocycloalkyl groups, such as C5-C7 heterocycloalkyl groups, and which have at least one hetero atom in the cyclic ring, such as, but not limited to, O, S, N, P, and combinations thereof.
  • heterocycloalkyl groups include, but are not limited to, imidazolyl, tetrahydrofuranyl, tetrahydropyranyl, piperidinyl, morpholinyl, and piperazinyl.
  • heterocycloalkyl as used herein also includes: bridged ring polycyclic heterocycloalkyl groups, such as, but not limited to, 7-oxabicyclo[2.2.1]heptanyl; and fused ring polycyclic heterocycloalkyl groups, such as, but not limited to, octahydrocyclopenta[b]pyranyl, and octahydro- IH-isochromenyl.
  • nitrogen-containing heterocycle means a cyclic ring that includes at least one nitrogen atom in the ring, such as one or two nitrogen atoms, and optionally at least one additional heteroatom that is other than nitrogen, such as oxygen, and which with some embodiments is covalently bonded to another group, such as an indenonaphthopyran compound according to the present invention, through a nitrogen atom in the ring.
  • nitrogen-containing heterocycles include, but are not limited to: cyclic aminos, such as piperidino, pyrrolidino, piperazino, and morpholino; cyclic amides (or lactams), such as C3-C6 cyclic amides, such as P-propiolactam, y-butyrolactam, 5-valerolactam, or s-caprolactam; and heteroaromatics, such as imidazole, pyrrole, indole, and carbazole.
  • cyclic aminos such as piperidino, pyrrolidino, piperazino, and morpholino
  • cyclic amides (or lactams) such as C3-C6 cyclic amides, such as P-propiolactam, y-butyrolactam, 5-valerolactam, or s-caprolactam
  • heteroaromatics such as imidazole, pyrrole, indole,
  • alkyl groups cycloalkyl groups, heterocycloalkyl groups, haloalkyl groups, and the like, are also applicable to alkane groups, cycloalkane groups, heterocycloalkane groups, haloalkane groups, etc., such as, but not limited to, polyvalent alkane groups, such as polyvalent alkane linking groups, such as divalent alkane linking groups.
  • aryl and related terms, such as “aryl group”, means an aromatic cyclic monovalent hydrocarbon radical.
  • aromatic and related terms, such as “aromatic group,” means a cyclic conjugated hydrocarbon having stability (due to delocalization of pi-electrons) that is significantly greater than that of a hypothetical localized structure.
  • aryl groups include Ce-Cu aryl groups, such as, but not limited to, phenyl, naphthyl, phenanthryl, and anthracenyl.
  • heteroaryl includes, but is not limited to, C3-C18 heteroaryl, such as, but not limited to, C3-C10 heteroaryl (including fused ring polycyclic heteroaryl groups) and means an aryl group having at least one hetero atom in the aromatic ring, or in at least one aromatic ring in the case of a fused ring polycyclic heteroaryl group.
  • heteroaryl groups include, but are not limited to, furanyl, pyranyl, pyridinyl, quinolinyl, isoquinolinyl, and pyrimidinyl.
  • Representative alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, neopentyl, hexyl, heptyl, octyl, nonyl and decyl.
  • Representative alkenyl groups include, but are not limited to, vinyl, allyl, and propenyl.
  • Representative alkynyl groups include, but are not limited to, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, and 2-butynyl.
  • Representative cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl.
  • halo and related terms, such as “halo group,” “halo substituent,” “halogen group,” and “halogen substituent,” means a single bonded halogen group, such as -F, -Cl, -Br, and -I.
  • halo substituted and related terms (such as, but not limited to, haloalkyl groups, haloalkenyl groups, haloalkynyl groups, haloaryl groups, and halo-heteroaryl groups) means a group in which at least one, and up to and including all of the available hydrogen groups thereof is substituted with a halo group, such as, but not limited to F, Cl or Br.
  • halo-substituted is inclusive of “perhalo-substituted.”
  • perfluoroalkyl group means an alkyl group in which all available hydrogen groups thereof have in each case been substituted (or replaced) with a fluoro (F) group.
  • “at least one of’ is synonymous with “one or more of,” whether the elements are listed conjunctively or disjunctively.
  • the phrases “at least one of A, B, and C” and “at least one of A, B, or C” each mean any one of A, B, or C, or any combination of any two or more of A, B, or C.
  • selected from is synonymous with “chosen from” whether the elements are listed conjunctively or disjunctively.
  • the phrases “selected from A, B, and C” and “selected from A, B, or C” each mean any one of A, B, or C, or any combination of any two or more of A, B, or C. For example, A alone; or B alone; or C alone; or A and B; or A and C; or B and C; or all of A, B, and C.
  • ketone such as with regard to groups, and substituents of various groups, of the photochromic compounds of the present invention, and related terms, such as “ketone group” and “ketone substituent”, includes a material represented by -C(O)R, where R is selected from those groups as described below.
  • the term “carboxylic acid” such as with regard to groups, and substituents of various groups, of the photochromic compounds of the present invention, and related terms, such as “carboxylic acid group” and “carboxylic acid substituent” includes a material represented by -C(O)OH.
  • esters such as with regard to groups, and substituents of various groups, of the compounds and components of the present invention, and related terms, such as “ester group” and “ester substituent” means a carboxylic acid ester group represented by -C(O)OR, where R is selected from those groups as described below.
  • carbonate such as with regard to groups, and substituents of various groups, of the compounds and components of the present invention, and related terms, such as “carbonate group” and “carbonate substituent” includes a material represented by -OC(O)OR, where R is selected from those groups as described below.
  • urethane such as with regard to groups, and substituents of various groups, of the compounds and components of the present invention, and related terms, such as “urethane group,” and “urethane substituent,” includes a material represented by -OC(O)N(R)(H) or -N(H)C(O)OR, where R in each case is independently selected from those groups as described below.
  • each R group of each of the above described ketone, ester (carboxylic acid ester), carbonate, and urethane groups is in each case independently selected from alkyl, haloalkyl, perhaloalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, and combinations thereof (including those classes and examples thereof as recited previously herein).
  • the indenonaphthopyran compounds according to the present invention such as, but not limited to those represented by Formula (I), and the various groups thereof are described in further detail herein as follows.
  • substituted group means a group including, but not limited to, alkyl group, heterocycloalkyl group, aryl group, and/or heteroaryl group, in which at least one hydrogen thereof has been replaced or substituted with a group that is other than hydrogen.
  • substituents of the “substituted” groups of the indenonaphthopyran compounds according to the present invention are in each case independently selected from: alkoxy groups; halo groups (e.g., F, Cl, I, and Br); hydroxyl groups; thiol groups; alkylthio groups; arylthio groups; ketone groups; aldehyde groups; ester groups; carboxylic acid groups; cyano groups; alkyl groups; alkenyl groups; alkynyl groups; haloalkyl groups; perhaloalkyl groups; cycloalkyl groups; heterocycloalkyl groups; aryl groups (including alkaryl groups, including hydroxyl substituted aryl, such as phenol, and including poly-fused-ring aryl); heteroaryl groups (including poly-fused-ring heteroaryl groups); amino groups, such as -N(R n )(R 12 ) where R 11 and R 12 are each independently selected from: alkoxy
  • the substituents of the “substituted” groups of the indenonaphthopyran compounds according to the present invention are in each case independently selected from: alkoxy groups; halo groups (e.g., F, Cl, I, and Br); hydroxyl groups; thiol groups; ketone groups; aldehyde groups; ester groups; carboxylic acid groups; cyano groups; alkyl groups; haloalkyl groups; perhaloalkyl groups; cycloalkyl groups; heterocycloalkyl groups; aryl groups; and heteroaryl groups.
  • the substituents of a substituted group are more particularly recited.
  • m is from 0 to 3 (such as, 0, 1, 2, or 3); and n is from 0 to 3 (such as, 0, 1, 2, or 3).
  • at least one of m and n is at least 1.
  • m is 1 and/or n is 1.
  • n is 1.
  • R 1 is aryl substituted with at least one perfluoroalkyl group, or heteroaryl substituted with at least one perfluoroalkyl group.
  • R 1 is aryl substituted with at least one linear or branched Ci-Cio perfluoroalkyl group, or heteroaryl substituted with at least one linear or branched Ci-Cio perfluoroalkyl group.
  • R 2 is alkoxy.
  • R 2 is alkoxy
  • recitations of “R 2 is alkoxy,” and the like, means that the oxygen of the alkoxy group is bonded to Position-6 of the indenonaphthopyran represented by Formula (I).
  • R 2 is linear or branched Ci-Cio alkoxy.
  • R 3 is alkoxy, amino, or substituted or unsubstituted nitrogen-containing heterocycle.
  • R 3 is other than alkoxy (i.e., amino, or substituted or unsubstituted nitrogen-containing heterocycle)
  • R 3 is covalently bonded to position-7 by a nitrogen atom.
  • recitations of “R 3 is alkoxy,” and the like means that the oxygen of the alkoxy group is bonded to Position-7 of the indenonaphthopyran represented by Formula (I).
  • R 3 is selected from amino, or substituted or unsubstituted nitrogen-containing heterocycle (and not selected from alkoxy).
  • R 3 of Formula (I) is selected from linear or branched Ci-Cio alkoxy.
  • R 3 is, with some embodiments, selected from secondary or tertiary amino represented by the following Formula (II),
  • R 8 and R 9 are each independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, or substituted or unsubstituted aryl, provided that at least one of R 8 and R 9 is other than hydrogen.
  • R 3 is, with some embodiments, a nitrogen-containing hetrocycle selected from: substituted or unsubstituted piperidino (where the ring nitrogen thereof is covalently bonded to Position-7); substituted or unsubstituted morpholino (where the ring nitrogen thereof is covalently bonded to Position-7); and substituted or unsubstituted C3-C6 cyclic amide (where the ring / amide nitrogen thereof is covalently bonded to Position-7).
  • R 3 group of Formula (I), with some embodiments, is selected from a substituted or unsubstituted piperazino represented by the following Formula (III),
  • R 10 is selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl, alkyl sulfonyl, or perhaloalkyl sulfonyl.
  • R 4 and R 5 are each independently selected from: substituted or unsubstituted alkyl; or R 4 and R 5 together form a substituted or unsubstituted spirocyclic ring. With some further embodiments, R 4 and R 5 together form a spirocyclic ring that is fully carbocyclic (containing only carbon atoms in the spirocyclic ring), such as a C3-C10 spirocyclic ring, or a Cs-Cs spirocyclic ring. With some additional embodiments, R 4 and R 5 together form an unsubstituted spirocyclic ring. With some embodiments, R 4 and R 5 are each independently selected from unsubstituted linear or branched Ci-Ce alkyl.
  • R 6 independently for each n, and R 7 independently for each m, in each case are independently selected from: amino; substituted or unsubstituted nitrogen-containing heterocycle; a halo group; substituted or unsubstituted alkyl; substituted or unsubstituted alkoxy; perfluoroalkyl; or substituted or unsubstituted alkylthio.
  • R 6 independently for each n, and R 7 independently for each m are independently selected from: substituted or unsubstituted piperidino; substituted or unsubstituted morpholino; substituted or unsubstituted piperazino independently as described with reference to Formula (III) above and further herein; fluoro, chloro, or bromo; substituted or unsubstituted linear or branched Ci-Cis alkyl; substituted or unsubstituted linear or branched Ci-Ce alkyl; substituted or unsubstituted linear or branched Ci-Cis alkoxy; or substituted or unsubstituted linear or branched Ci-Ce alkoxy.
  • R 1 is phenyl substituted with at least one linear or branched C1-C4 perfluoroalkyl group, pyrdinyl substituted with at least one linear or branched C1-C4 perfluoroalkyl group, or pyrimidinyl substituted with at least one linear or branched C1-C4 perfluoroalkyl group.
  • R 2 of Formula (I) is linear or branched C1-C4 alkoxy.
  • R 3 is selected from, linear or branched Ci-Ce alkoxy.
  • R 3 is selected from a secondary or tertiary amino represented by Formula (II), where for Formula (II), R 8 and R 9 are each independently selected from hydrogen, substituted or unsubstituted linear or branched Ci-Ce alkyl, substituted or unsubstituted C5-C7 cycloalkyl, or substituted or unsubstituted aryl, provided that at least one of R 8 and R 9 is other than hydrogen.
  • R 3 is selected from: unsubstituted piperidino; substituted or unsubstituted morpholino; or unsubstituted C3-C6 cyclic amide. Additionally, and in accordance with some embodiments, R 3 is selected from substituted or unsubstituted piperazino represented by Formula (III), wherein for Formula (III): R 10 is selected from hydrogen; substituted or unsubstituted linear or branched Ci-Ce alkyl; substituted or unsubstituted phenyl; or linear or branched Ci-Ce perhaloalkyl sulfonyl.
  • R 3 is selected from: linear or branched C1-C4 alkoxy; substituted or unsubstituted piperidino; substituted or unsubstituted morpholino; or unsubstituted C3-C6 cyclic amide.
  • R 3 is selected from, secondary or tertiary amino represented by Formula (II), where for Formula (II), R 8 and R 9 are each independently selected from unsubstituted linear or branched C1-C4 alkyl, or linear or branched C1-C4 perhaloalkyl, provided that at least one of R 8 and R 9 is linear or branched C1-C4 perhaloalkyl.
  • R 3 is selected from, a substituted piperazino represented by Formula (III), where for Formula (III), R 10 is selected from substituted or unsubstituted linear or branched C1-C4 alkyl, substituted or unsubstituted phenyl, or linear or branched C1-C4 perhaloalkyl sulfonyl.
  • R 10 is selected from substituted or unsubstituted linear or branched C1-C4 alkyl, substituted or unsubstituted phenyl, or linear or branched C1-C4 perhaloalkyl sulfonyl.
  • R 4 and R 5 are each independently selected from unsubstituted linear or branched C1-C4 alkyl.
  • R 6 independently for each n, and R 7 independently for each m are independently selected from: unsubstituted piperidino; unsubstituted morpholino; fluoro, chloro, or bromo; unsubstituted linear or branched C1-C4 alkyl; or unsubstituted linear or branched C1-C4 alkoxy.
  • At least one of R 6 and R 7 is unsubstituted linear or branched Ci-Cis alkoxy, or unsubstituted linear or branched Ci-Ce alkoxy, or unsubstituted linear or branched C1-C4 alkoxy.
  • R 1 is selected from: 4-(trifluoromethyl)phenyl; 2-(trifluoromethyl)phenyl; 2,4-bis(trifluoromethyl)phenyl; 3,5-bis(trifluoromethyl)phenyl; 3,4-bis(trifluoromethyl)phenyl; or 5- (trifluoromethyl)pyridine-2-yl.
  • R 2 is selected from, methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, or branched butoxy, such as t-butoxy; and R 3 is selected from, morpholino, 2,6-dimethylmorpholino, 4-phenylpiperazino, 4-(tri fluoromethyl )sulfonyl piperazino, y-butyrolactam, 5- valerolactam, or s-caprolactam.
  • R 4 and R 5 are each independently selected from methyl, ethyl, n-propyl, iso-propyl, n- butyl, or branched butyl, such as t-butyl; and R 6 and R 7 are each independently selected from methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, or branched butoxy, such as t-butoxy.
  • R 1 is selected from: 4-(trifluoromethyl)phenyl; 2-(trifluoromethyl)phenyl; 2,4-bis(trifluoromethyl)phenyl; 3,5-bis(trifluoromethyl)phenyl; 3,4-bis(trifluoromethyl)phenyl; or 5- (trifluoromethyl)pyridine-2-yl.
  • R 2 is methoxy; and R 3 is selected from, morpholino, 2,6-dimethylmorpholino, 4- phenylpiperazino, 4-(trifluoromethyl)sulfonyl piperazino, y-butyrolactam, 5- valerolactam, or s-caprolactam.
  • R 4 and R 5 are each n-propyl; and R 6 and R 7 are each independently selected from methoxy or n-butoxy.
  • indenonaphthopyran compounds according to the present invention can be prepared in accordance with art-recognized methods.
  • the indenonaphthopyran compound of the present invention is, with some embodiments, a photochromic indenonaphthopyran compound.
  • a photochromic composition which includes at least one indenonaphthopyran compound according to the present invention, which is a photochromic indenonaphthopyran compound, such as represented by Formula (I).
  • the photochromic indenonaphthopyran compounds of the present invention can be used in combination with a mixture of other photochromic compounds.
  • mixtures of photochromic compounds can be used to attain certain activated colors, such as a near neutral gray or near neutral brown. See, for example, U.S. Patent No. 5,645,767, col. 12, line 66 to col. 13, line 19, which describes the parameters that define neutral gray and brown colors.
  • Examples of classes of other photochromic compounds that can be used in combination with the photochromic indenonaphthopyran compounds of the present invention include, but are not limited to, indeno-fused naphthopyrans, naphtho[l,2- b]pyrans, naphtho[2,l-b]pyrans, spirofluoroeno[l,2-b]pyrans, phenanthrenopyrans, quinolinopyrans, fluoroanthenopyrans, spiropyrans, benzoxazines, naphthoxazines, spiro(indoline)naphthoxazines, spiro(indoline)pyridobenzoxazines, spiro(indoline)fluoranthenoxazines, spiro(indoline)quinoxazines, fulgides, fulgimides, diarylethenes, diarylalkylethenes, diary
  • the photochromic compositions of the present invention can, with some embodiments, further include one or more fixed-tint dyes.
  • fixed-tint dye and related terms, such as “fixed-colorant,” “static colorant,” “fixed dye,” and “static dye” means dyes that are: non-photosensitive materials, which do not physically or chemically respond to electromagnetic radiation with regard to the visually observed color thereof.
  • fixed-tint dye and related terms as used herein does not include and is distinguishable from photochromic compound.
  • non-photosensitive materials means materials that do not physically or chemically respond to electromagnetic radiation with regard to the visually observed color thereof, including, but not limited to, fixed-tint dyes.
  • One or more fixed-tint dyes can be present in the photochromic compositions of the present invention for purposes including, but not limited to, providing a article prepared from the photochromic compositions with: at least a base (or first) color characteristic of the fixed-tint dye, when the photochromic compound is not activated; and optionally a second color characteristic of the combination of the fixed-tint dye and the photochromic compound when activated, such as by exposure to actinic radiation.
  • the optional fixed-tint dye of the photochromic composition includes at least one of azo dyes, anthraquinone dyes, xanthene dyes, azime dyes, iodine, iodide salts, polyazo dyes, stilbene dyes, pyrazolone dyes, triphenylmethane dyes, quinoline dyes, oxazine dyes, thiazine dyes, and polyene dyes.
  • the fixed-tint dye can be present in the photochromic composition in varying amounts to provide the intended effect in the cured article prepared therefrom.
  • the fixed-tint dye is present in the photochromic composition in an amount of from 0.001 to 15 percent by weight, or from 0.01 to 10 percent by weight, or from 0.1 to 2.5 percent by weight, the percent weights in each case being based on the total resin solids weight of the photochromic composition.
  • the photochromic composition includes: (i) a matrix forming material, in which the matrix forming material is at least one of a polymeric material, an oligomeric material, and/or a monomeric material; and (ii) the indenonaphthopyran compound according to the present invention, which is a photochromic indenonaphthopyran compound, such as represented by Formula (I).
  • the photochromic indenonaphthopyran compound can be incorporated into a portion of the organic material by methods including, but not limited to, at least one of blending or bonding the photochromic compound with the organic material or a precursor of the organic material.
  • the terms “blending” and “blended” mean that the photochromic compound/material is intermixed or intermingled with the at least a portion of the organic material, but not bonded to the organic material.
  • the terms “bonding” or “bonded” mean that the photochromic compound/material is linked, such as by one or more covalent bonds, to a portion of the organic material or a precursor thereof.
  • the photochromic material can be linked to the organic material through a reactive substituent, such as, but not limited to a hydroxyl group, a primary amine group, and/or a secondary amine group.
  • the photochromic compound can be incorporated into at least a portion of the polymeric material or at least a portion of the monomeric material or oligomeric material from which the polymeric material is formed.
  • photochromic compound(s) according to the present invention that have a reactive substituent can be bonded to an organic material such as a monomer, oligomer, or polymer having a group with which a reactive moiety may be reacted, or the reactive moiety can be reacted as a co-monomer in the polymerization reaction from which the organic material is formed, for example, in a co-polymerization process.
  • the photochromic compositions according to present invention can include an organic material chosen from a polymeric material, an oligomeric material and/or a monomeric material, with some embodiments.
  • polymeric materials that can be used with the photochromic compositions of the present invention include, but are not limited to: poly(carbonate); copolymers of ethylene and vinyl acetate; copolymers of ethylene and vinyl alcohol; copolymers of ethylene, vinyl acetate, and vinyl alcohol (such as those that result from the partial saponification of copolymers of ethylene and vinyl acetate); cellulose acetate butyrate; poly(urethane); poly(acrylate); poly(methacrylate); epoxies; aminoplast functional polymers; poly(anhydride); poly(urea urethane); N-alkoxymethyl(meth)acrylamide functional polymers; poly(siloxane); poly(silane); and combinations and mixtures thereof.
  • the photochromic composition of the present invention can include at least one of, a complementary photochromic material (including one or more of those other photochromic materials and compounds described previously herein), a photoinitiator, a thermal initiator, a polymerization inhibitor, a solvent, a light stabilizer, a heat stabilizer, a mold release agent, a rheology control agent, a leveling agent, a free radical scavenger, and/or an adhesion promoter.
  • a complementary photochromic material including one or more of those other photochromic materials and compounds described previously herein
  • a photoinitiator including one or more of those other photochromic materials and compounds described previously herein
  • a photoinitiator including one or more of those other photochromic materials and compounds described previously herein
  • a photoinitiator including one or more of those other photochromic materials and compounds described previously herein
  • a photoinitiator including one or more of those other photochromic materials and compounds described previously herein
  • the photochromic composition according to the present invention can be a photochromic coating composition.
  • Photochromic coating compositions of the present invention can include: a photochromic compound according to the present invention, such as described previously herein with regard to Formula (I); a resin composition that is optionally curable; and optionally a solvent.
  • the photochromic coating composition can be in the form of art-recognized liquid coatings and powder coatings.
  • the photochromic coating compositions of the present invention can be thermoplastic or curable (e.g., thermosetting and/or photosetting) coating compositions.
  • the curable resin composition of the curable photochromic coating compositions according to the present invention can include: a first reactant (or component) having functional groups, e.g., an epoxide functional polymer reactant; and a second reactant (or component) that is a crosslinking agent having functional groups that are reactive towards and that can form covalent bonds with the functional groups of the first reactant.
  • the first and second reactants of the curable resin composition of the curable photochromic coating composition can each independently include one or more functional species, and are each present in amounts sufficient to provide cured photochromic coatings having a desirable combination of physical properties, e.g., smoothness, optical clarity, solvent resistance, and hardness.
  • epoxide functional polymer e.g., (meth)acrylic polymers containing residues of glycidyl (meth)acrylate
  • epoxide reactive crosslinking agent e.g., containing active hydrogens, such as hydroxyls, thiols and amines
  • capped (or blocked) isocyanate functional crosslinking agent is meant a crosslinking agent having two or more capped isocyanate groups that can decap (or deblock) under cure conditions (e.g., at elevated temperature) to form free isocyanate groups and free capping groups.
  • the free isocyanate groups formed by decapping of the crosslinking agent are preferably capable of reacting and forming substantially permanent covalent bonds with the active hydrogen groups of the active hydrogen functional polymer (e.g., with the hydroxy groups of a hydroxy functional polymer).
  • Curable photochromic coating compositions according to the present invention can, optionally, contain additives such as waxes for flow and wetting, flow control agents, e.g., poly(2-ethylhexyl)acrylate, adjuvant resin to modify and optimize coating properties, antioxidants and ultraviolet (UV) light absorbers.
  • flow control agents e.g., poly(2-ethylhexyl)acrylate
  • adjuvant resin to modify and optimize coating properties
  • antioxidants and ultraviolet (UV) light absorbers examples include those available commercially from BASF under the trademarks IRGANOX and TINUVIN.
  • UV light absorbers include those available commercially from BASF under the trademarks IRGANOX and TINUVIN.
  • These optional additives, when used, are typically present in amounts up to 20 percent by weight (e.g., from 0.5 to 10 percent by weight), based on total weight of resin solids of the curable resin composition.
  • Photochromic compositions, photochromic articles and photochromic coating compositions according to the present invention can further include art-recognized additives that aid or assist in the processing and/or performance of the compositions or articles.
  • additives include photoinitiators, thermal initiators, polymerization inhibitors, solvents, light stabilizers (such as, but not limited to, ultraviolet light absorbers and light stabilizers, such as hindered amine light stabilizers (HALS)), heat stabilizers, mold release agents, rheology control agents, leveling agents (such as, but not limited to, surfactants), free radical scavengers, adhesion promoters (such as hexanediol diacrylate and coupling agents), and combinations and mixtures thereof.
  • light stabilizers such as, but not limited to, ultraviolet light absorbers and light stabilizers, such as hindered amine light stabilizers (HALS)
  • HALS hindered amine light stabilizers
  • leveling agents such as, but not limited to,
  • the photochromic compositions of the present invention can, with some embodiments, include one or more solvents, such as one or more organic solvents.
  • Classes of organic solvents that can be present in the photochromic compositions of the present invention include, but are not limited to: ketones, such as, acetone, methyl ethyl ketone, and methyl isobutyl ketone; ethers, such as, dimethyl ether and methyl ethyl ether; cyclic ethers, such as, tetrahydrofuran and dioxane; esters, such as, ethyl acetate, ethyl lactate, ethylene carbonate and propylene carbonate; nitrogen containing cyclic compounds, such as, pyrrolidone, N-methyl-2-pyrrolidone, 1-butyl- pyrrolidinone, and l,3-dimethyl-2-imidazolidinone; sulfur containing compounds, such as, dimethyl sulfoxide and tetramethylene sulfone; aromatic compounds, such as, toluene, xylene, anisole, and but
  • Solvent(s) can be present in the photochromic compositions of the present invention, in an amount of from 5 to 95 percent by weight, or from 15 to 80 percent by weight, from 30 to 70 percent by weight, or from 30 to 60 percent by weight, in each case based on the total weight of the photochromic composition (including the weight of the solvent).
  • the photochromic compounds of the present invention can be used in amounts (or ratios) such that the compositions, organic material or substrate (e.g., photochromic articles and photochromic coatings) into which the photochromic compounds are incorporated or otherwise connected exhibits desired optical properties.
  • the amount and types of photochromic material can be selected such that the composition, organic material or substrate is clear or colorless when the photochromic compound is in the closed-form (e.g., in the bleached or unactivated state), and can exhibit a desired resultant color when the photochromic compound (such as a photochromic indeno-fused naphthopyran of the present invention) is in the open -form (e.g., when activated by actinic radiation).
  • Photochromic compositions according to the present invention can include the photochromic compound according to the present invention, including the compounds represented by Formula (I) in an amount of from 0.01 to 40 weight percent, such as from 0.05 to 15 weight percent, such as from 0.1 to 5 weight percent, based on the weight of the photochromic composition.
  • the amount of the photochromic compound/material including the compound(s) represented by Formula (I), that is incorporated into an organic material can range from 0.01 to 40 weight percent, such as from 0.05 to 15 weight percent, such as from 0.1 to 5 weight percent, based on the weight of the organic material.
  • the present invention also relates to photochromic articles that include one or more photochromic compounds according to the present invention, such as represented by Formula (I).
  • the photochromic articles can be prepared by art-recognized methods, such as, but not limited to, by imbibition methods, cast-in-place methods, coating methods, in-mold coating methods, over-mold methods, and lamination methods.
  • the photochromic articles can be selected from ophthalmic articles, display articles, windows, mirrors, active liquid crystal cell articles, and passive liquid crystal cell articles.
  • the photochromic articles of the present invention can be ophthalmic articles, and the ophthalmic articles can be selected from corrective lenses, non-corrective lenses, contact lenses, intra-ocular lenses, magnifying lenses, protective lenses, and visors.
  • the photochromic articles of the present invention can, with some further embodiments, be display articles, and the display articles can be selected from screens, monitors, and security elements.
  • the present invention can be further characterized by one or more of the following non-limiting aspects.
  • Aspect 1 An indenonaphthopyran compound represented by the following Formula (I),
  • n is from 0 to 3;
  • R 1 is aryl substituted with at least one perfluoroalkyl group, or heteroaryl substituted with at least one perfluoroalkyl group;
  • R 2 is alkoxy
  • R 3 is alkoxy, amino, or substituted or unsubstituted nitrogen-containing heterocycle, wherein when R 3 is other than alkoxy, R 3 is covalently bonded to position-7 by a nitrogen atom;
  • R 4 and R 5 are each independently selected from, substituted or unsubstituted alkyl; or
  • R 4 and R 5 together form a substituted or unsubstituted spirocyclic ring
  • R 6 independently for each n, and R 7 independently for each m, in each case are independently selected from, amino; substituted or unsubstituted nitrogen-containing heterocycle; a halo group; substituted or unsubstituted alkyl; substituted or unsubstituted alkoxy; perfluoroalkyl; or substituted or unsubstituted alkylthio.
  • Aspect 2 The indenonaphthopyran compound of aspect 1 wherein,
  • R 1 is aryl substituted with at least one linear or branched Ci-Cio perfluoroalkyl group, or heteroaryl substituted with at least one linear or branched Ci-Cio perfluoroalkyl group;
  • R 2 is linear or branched Ci-Cio alkoxy
  • R 3 is selected from, linear or branched Ci-Cio alkoxy, secondary or tertiary amino represented by the following Formula (II), wherein for Formula (II), R 8 and R 9 are each independently selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, or substituted or unsubstituted aryl, provided that at least one of R 8 and R 9 is other than hydrogen, substituted or unsubstituted piperidino, substituted or unsubstituted morpholino, substituted or unsubstituted C3-C6 cyclic amide, or substituted or unsubstituted piperazino represented by the following Formula (III), wherein for Formula (III),
  • R 10 is selected from hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted aryl, alkyl sulfonyl, or perhaloalkyl sulfonyl.
  • Aspect 3 The indenonaphthopyran compound of aspect 2 wherein, R 1 is aryl substituted with at least one linear or branched Ci-Ce perfluoroalkyl group, or heteroaryl substituted with at least one linear or branched Ci-Ce perfluoroalkyl group;
  • R 2 is linear or branched Ci-Ce alkoxy
  • R 3 is selected from, linear or branched Ci-Ce alkoxy, secondary or tertiary amino represented by Formula (II), wherein for Formula (II), R 8 and R 9 are each independently selected from hydrogen, substituted or unsubstituted linear or branched Ci-Ce alkyl, substituted or unsubstituted C5-C7 cycloalkyl, or substituted or unsubstituted aryl, provided that at least one of R 8 and R 9 is other than hydrogen, unsubstituted piperidino, substituted or unsubstituted morpholino, unsubstituted C3-C6 cyclic amide, or substituted or unsubstituted piperazino represented by Formula (III), wherein for Formula (III),
  • R 10 is selected from hydrogen, substituted or unsubstituted linear or branched Ci-Ce alkyl, substituted or unsubstituted phenyl, or linear or branched Ci-Ce perhaloalkyl sulfonyl,
  • R 4 and R 5 are each independently selected from, unsubstituted linear or branched Ci-Ce alkyl
  • R 6 independently for each n, and R 7 independently for each m, in each case are independently selected from, substituted or unsubstituted piperidino, substituted or unsubstituted morpholino, substituted or unsubstituted piperazino independently as described with reference to Formula (III), fluoro, chloro, or bromo, substituted or unsubstituted linear or branched Ci-Ce alkyl, or substituted or unsubstituted linear or branched Ci-Ce alkoxy.
  • Aspect 4 The indenonaphthopyran compound of aspect 2 or aspect 3 wherein, R 1 is phenyl substituted with at least one linear or branched C1-C4 perfluoroalkyl group, or pyridinyl substituted with at least one linear or branched C1-C4 perfluoroalkyl group;
  • R 2 is linear or branched C1-C4 alkoxy
  • R 3 is selected from, linear or branched C1-C4 alkoxy, secondary or tertiary amino represented by Formula (II), wherein for Formula (II), R 8 and R 9 are each independently selected from unsubstituted linear or branched C1-C4 alkyl, or linear or branched C1-C4 perhaloalkyl, provided that at least one of R 8 and R 9 is linear or branched C1-C4 perhaloalkyl, substituted or unsubstituted piperidino, substituted or unsubstituted morpholino, substituted piperazino represented by Formula (III), wherein for Formula (III),
  • R 10 is selected from substituted or unsubstituted linear or branched C1-C4 alkyl, substituted or unsubstituted phenyl, or linear or branched C1-C4 perhaloalkyl sulfonyl, or unsubstituted C3-C6 cyclic amide;
  • R 4 and R 5 are each independently selected from, unsubstituted linear or branched C1-C4 alkyl
  • R 6 independently for each n, and R 7 independently for each m, in each case are independently selected from, unsubstituted piperidino, unsubstituted morpholino, fluoro, chloro, or bromo, unsubstituted linear or branched C1-C4 alkyl, or unsubstituted linear or branched C1-C4 alkoxy.
  • Aspect 5 The indenonaphthopyran compound of any one of aspects 1 to 4, provided that at least one of R 6 and R 7 is unsubstituted linear or branched C1-C4 alkoxy.
  • Aspect 6 The indenonaphthopyran compound of any one of aspects 1 to 5, wherein,
  • R 1 is selected from,
  • R 2 is selected from, methoxy, or ethoxy
  • R 3 is selected from, morpholino
  • R 4 and R 5 are each independently selected from, methyl, ethyl, n-propyl, iso-propyl, n-butyl, or branched butyl, such as t-butyl;
  • R 6 and R 7 are each independently selected from, methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, or branched butoxy, such as t-butoxy.
  • Aspect 7 The indenonaphthopyran compound of any one of aspects 1 to 6, wherein,
  • R 1 is selected from,
  • R 2 is methoxy
  • R 3 is selected from, morpholino
  • R 4 and R 5 are each n-propyl
  • a photochromic composition comprising the indenonaphthopyran compound of any one of aspects 1 to 7.
  • a photochromic article comprising the indenonaphthopyran compound of any one of aspects 1 to 7, wherein the photochromic article is selected from the group consisting of ophthalmic articles, display articles, windows, mirrors, active liquid crystal cell articles, and passive liquid crystal cell articles.
  • Aspect 10 The photochromic article of aspect 9, wherein the photochromic article is selected from ophthalmic articles, and the ophthalmic articles are selected from corrective lenses, non-corrective lenses, contact lenses, intra-ocular lenses, magnifying lenses, protective lenses, and visors.
  • Part-1 of the following examples there are provided descriptions of the synthetic preparation of comparative indenonaphthopyran compounds (Comparative Examples / Compounds CE1, CE2, CE12, and CE13) and indenonaphthopyran compounds according to the present invention (Examples / Compounds 3-11, 14, and 15).
  • Part-2 there is provided a summary of an evaluation of the comparative and inventive indenonaphthopyran compounds of Part- 1.
  • Scheme-1 provides a summary, in particular, of the synthesis of the indenonaphthopyran compound of Comparative Example 1 (CE1).
  • Scheme-1 also includes starting materials, and/or intermediates, and/or alternative species thereof that were used to synthesize other comparative and inventive compounds in the following examples.
  • a comparative compound, CE1 was prepared in accordance with the following steps.
  • reaction mixture was allowed to warm to room temperature and then stirred for 16 hours. It was then poured into ice water and extracted twice with ethyl acetate. The combined organic layers were washed with brine twice, dried over sodium sulfate, and concentrated to dryness. The resulting residue was filtered over a short plug of silica gel and the filter was washed with a mixture of 25% ethyl acetate and 75% hexanes. The mother liquor was concentrated to dryness resulting in an amber colored oil consistent with the intermediate product (103’) depicted below, and (103) in Scheme-1 (25.02 g).
  • each of the of the indenonaphthopyran compounds of Part- 1 were incorporated into a polyurethane coating system as described in US Pat. No. 8,608,988 B2, examples 1-3 at the same mole % and applied at the same coating thickness on 2” x 2” (5.1 cm x 5.1 cm) test chips made from CR-39® monomer (PPG Industries, Inc.). All coated test chips were cured at 125°C for 1 hour.
  • Each of the coated test chips was conditioned by first being exposed to 365 nanometer ultraviolet light for 10 minutes at a distance of about 14 centimeters to activate the photochromic materials within the coating.
  • the UVA (315 to 380 nm) irradiance at the chip was measured with a LICOR® Model Li- 1800 spectroradiometer and found to be 22.2 watts per square meter.
  • Each of the test chips was then placed under a 500 watt, high intensity halogen lamp for 10 minutes at a distance of about 36 centimeters to bleach (inactivate) the photochromic materials.
  • the illuminance at chip was measured with the LICOR® spectroradiometer and found to be 21.9 Klux.
  • the coated test chips then were kept in a dark environment at room temperature (i.e., from 70°F to 75°F, or 21°C to 24°C) for at least 1 hour prior to testing / measurement on an optical bench. Prior to optical bench measurement, the coated test chips were measured for ultraviolet absorbance at 390 nanometers.
  • Percent transmission (%T) for each of the coated test chips was determined using the CIE Y value in accordance with CIE 15: 2004 colorimetry using a D 65 illuminant and 10° observer.
  • the a* and b* values as used herein refers to the a* and b* values measured in accordance with CIE 15: 2004 space colorimetry, employing a D 65 illuminant and 10° observer, using an UltraScan Pro (Hunter Labs).
  • the BMP optical bench was fitted with two 150-watt ORIEL® Model #66057 Xenon arc lamps at right angles to each other.
  • the light path from Lamp 1 was directed through a 3 mm SCFIOTT® KG-2 band-pass filter and appropriate neutral density filters that contributed to the required UV and partial visible light irradiance level.
  • the light path from Lamp 2 was directed through a 3 mm SCFIOTT® KG-2 band-pass filter, a SCFIOTT® short band 400 nm cutoff filter and appropriate neutral density filters in order to provide supplemental visible light illuminance.
  • a 2 inch x 2 inch (5.1 cm x 5.1 cm) 50% polka dot beam splitter, at 45° to each lamp is used to mix the two beams.
  • the combination of neutral density filters and voltage control of the Xenon arc lamp were used to adjust the intensity of the irradiance.
  • Proprietary software i.e., BMPSoft version 2.1 e
  • BMPSoft version 2.1 e was used on the BMP to control timing, irradiance, air cell and sample temperature, shuttering, filter selection and response measurement.
  • the power output of the optical bench i.e., the dosage of light that the coated test chip was exposed to, was adjusted to 6.7 Watts per square meter (W/m 2 ) UVA, integrated from 315-380 nm and 50 Klux illuminance, integrated from 380-780 nm. Measurement of this power setpoint was made using an irradiance probe and the calibrated Zeiss spectrophotometer.
  • the coated test chip sample cell was fitted with a quartz window and self-centering sample holder. The temperature in the sample cell was controlled at 23 °C through the software with a modified Facis, Model FX-10, environment simulator.
  • Measurement of the coated test chips’ dynamic photochromic response and color measurements was made using the same Zeiss spectrophotometer, with fiber optic cables for light delivery from a tungsten halogen lamp and through the sample.
  • the collimated monitoring light beam from the fiber optic cable was maintained perpendicular to the test sample while passing through the coated test chip sample and directed into a receiving fiber optic cable assembly attached to the spectrophotometer.
  • the exact point of placement of the coated test chip sample in the sample cell was where the activating xenon arc beam and the monitoring light beam intersected to form two concentric circles of light.
  • the angle of incidence of the xenon arc beam at the sample placement point was 30° from perpendicular.
  • % Tb is the percent transmission in the bleached state
  • % Ta is the percent transmission in the activated state.
  • the AOD at saturation is after 15 minutes of activation and the Fade Half Life (Tl/2) value is the time interval in seconds for the AOD of the activated form of the photochromic material in the coating to reach one half the fifteen minute AOD at 73.4°F (23 °C), after removal of the activating light source.
  • Table 3 [0121] The data summarized in Table 2 demonstrates that indenonaphthopyran compounds according to the present invention (having (perfluoroalkyl)aryl)thio substituents at Position-11) provide improved fade speed, as compared to comparative indenonaphthopyran compounds (having (fluoroaryl)thio substituents at Position-11), without a significant sacrifice in the darkness of the activated state.
  • the data summarized in Table 3 further demonstrates the fast fade speeds provided by indenonaphthopyran compounds according to the present invention having various groups at Position-7 and Position- 11 thereof.

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Abstract

La présente invention concerne des composés d'indénonaphtopyrane représentés par la formule (I) suivante, en référence à la formule (I), m, n et R4-R7 sont tels que décrits dans la description. Avec une autre référence à la formule (I), R1 est un aryle substitué par au moins un groupe perfluoroalkyle, ou un hétéroaryle substitué par au moins un groupe perfluoroalkyle; R2 est alcoxy; et R3 est alcoxy, amino, ou hétérocycle contenant de l'azote substitué ou non substitué, à condition que lorsque R3 est autre qu'alcoxy, R3 est lié de manière covalente à la position-7 par un atome d'azote. La présente invention concerne également des compositions photochromiques et des articles photochromiques qui comprennent des composés indénonaphtopyranes représentés par la formule (I).
PCT/EP2023/063277 2023-05-17 2023-05-17 Indénonaphtopyranes ayant un sulfure d'aryle/hétéroaryle à substitution perfluoroalkyle en position-11 Pending WO2024235463A1 (fr)

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AU2023448383A AU2023448383A1 (en) 2023-05-17 2023-05-17 Indenonaphthopyrans having perfluoroalkyl substituted aryl / heteroaryl sulfide at position-11

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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5645767A (en) 1994-11-03 1997-07-08 Transitions Optical, Inc. Photochromic indeno-fused naphthopyrans
EP2669278A1 (fr) * 2011-01-27 2013-12-04 Tokuyama Corporation Composé de chromène
EP2669277A1 (fr) * 2011-01-28 2013-12-04 Tokuyama Corporation Composé de chromène
US8608988B2 (en) 2010-11-23 2013-12-17 Transitions Optical, Inc. Curable photochromic compositions and optical articles prepared therefrom
EP2759543A1 (fr) * 2011-09-22 2014-07-30 Tokuyama Corporation Composé de chromène et composition durcissable
US9028728B2 (en) 2005-04-08 2015-05-12 Transitions Optical, Inc. Photochromic materials that include indeno-fused naphthopyrans
WO2016142496A1 (fr) 2015-03-10 2016-09-15 Transitions Optical, Ltd. Élément optique ayant un revêtement pour visibilité améliorée d'un repère et procédé de fabrication de l'élément optique
WO2017030545A1 (fr) 2015-08-17 2017-02-23 Transitions Optical, Inc. Compositions photochromiques durcissables

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5645767A (en) 1994-11-03 1997-07-08 Transitions Optical, Inc. Photochromic indeno-fused naphthopyrans
US9028728B2 (en) 2005-04-08 2015-05-12 Transitions Optical, Inc. Photochromic materials that include indeno-fused naphthopyrans
US8608988B2 (en) 2010-11-23 2013-12-17 Transitions Optical, Inc. Curable photochromic compositions and optical articles prepared therefrom
EP2669278A1 (fr) * 2011-01-27 2013-12-04 Tokuyama Corporation Composé de chromène
EP2669277A1 (fr) * 2011-01-28 2013-12-04 Tokuyama Corporation Composé de chromène
EP2759543A1 (fr) * 2011-09-22 2014-07-30 Tokuyama Corporation Composé de chromène et composition durcissable
WO2016142496A1 (fr) 2015-03-10 2016-09-15 Transitions Optical, Ltd. Élément optique ayant un revêtement pour visibilité améliorée d'un repère et procédé de fabrication de l'élément optique
WO2017030545A1 (fr) 2015-08-17 2017-02-23 Transitions Optical, Inc. Compositions photochromiques durcissables

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