Rodenstock Gmbh

Optische Werke G. Rodenstock

Udo Weigand

Manfred Melzig

Claudia Mann

Yven Rohlfing

Herbert Zinner

The present invention relates to new photochromic, fused naphthopyran systems having specific substituents R, which can be used to attain very rapid lightening speeds, without detriment to the depth of darkening after excitation, and also to the use thereof in plastics of all kinds.

Photochromic annelated naphthopyrane systems with special substituents, for attaining rapid lightening speeds

The present invention relates to photochromic polyfused naphthopyrans having very long-wave absorption of the closed form extending well into the visible wavelength range, and to the use thereof in all kinds of plastics, especially for ophthalmic purposes, preferably in driving glasses.

Photochromic multiple ring-fused naphthopyrans having extreme longwave absorption extending far into the visible wavelength range

The present invention relates to UV-curing-compatible photochromic single- or double-fused naphthopyrans of the general formulae (I) or (II) and the use thereof in plastics of all kinds, particularly for ophthalmic purposes. The photochromic compounds according to the invention are characterized by their excellent UV-curing compatibility, i.e. they remain undamaged&#x2014;incorporated, for example, in an acrylate monomer matrix with UV initiator&#x2014;by a free-radical polymerization of the matrix initiated by strong UV light. The photochromic dyes according to the invention, by means of suitable choice of substituents, are in addition characterized by two distinct absorption bands of the open form in the visible wavelength range, i.e. two conventional photochromic dyes, each having one discrete absorption band, can be replaced with a molecule of this type.

UV-curing-compatible photochromic fused naphthopyrans

The present invention relates to photochromic fluorenopyrans with defined dibenzo[b,d]pyrano fusion in accordance with general formulae (I) or (II) and to their use in plastics of all kinds, particularly for ophthalmic purposes. The photochromic compounds of the invention are distinguished by two pronounced absorption bands of the open form in the visible wavelength range, meaning that with dye molecules of this kind it is possible to replace two conventional photochromic dyes each having only one discrete absorption band. The compounds of the invention, moreover, have a very good lifetime with very high performance.

Photochromic fluorenopyrans with defined dibenzo[B,D]pyrano fused attachment

The present invention relates to photochromic double-fused naphthopyrans of the general formula (I) or (II) and the use thereof in plastics of all kinds, particularly for ophthalmic purposes. The photochromic compounds according to the invention are characterized by two distinct absorption bands of the open form in the visible wavelength range, i.e. two conventional photochromic dyes, each having only one discrete absorption band, can be replaced with dye molecules of this type. The compounds according to the invention, moreover, have a very good lifetime with a very high performance.

Photochromic double-fused naphthopyrans

The present invention relates to photochromic double-indeno-fused naphthopyrans of the general formula (I) and the use thereof in plastics of all kinds, particularly for ophthalmic purposes. The photochromic compounds according to the invention are characterized by two distinct absorption bands of the open form in the visible wavelength range, i.e. two conventional photochromic dyes, each having only one discrete absorption band, can be replaced with dye molecules of this type. The compounds according to the invention, moreover, have a very good lifetime with a very high performance.

Photochromic bis-idenofused naphthopryans

The present invention relates to photochromic fused naphthopyrans having a benzene ring which is adjacent to the pyran oxygen and is linked to the para substituent via both meta positions, and to the use thereof in plastics of all types, in particular for ophthalmic purposes.

Photochromic fused naphthopyrans having a benzene ring which is adjacent to the pyran oxygen and is linked to the para substituent via both meta positions

The present invention relates to photochromic naphthopyrancs having a double-bridged terphenyl sub-unit, and to the use thereof in plastics of all types, particularly for ophthalmic purposes.

Photochromic naphthopyrans having a double-bridged terphenyl sub-unit

The present invention relates to photochromic benzopyranobenzopyrans with additional fusion and to the use thereof in plastics of all types, in particular for ophthalmic purposes. The compounds according to the invention are photochromic benzopyran compounds which can also be regarded as derived from 9-oxa-9,10-dihydrophenanthrene.

Photochromic benzopyrano-benzopyrans with further fusing

Specific photochromic spirodihydrophenanthropyrans and their use in synthetic resin materials of all kinds, particularly for ophthalmic purposes. The compounds of the invention are photochromic pyran compounds derived from 9,10-dihydrophenanthrene in which at least one of the two carbon atoms at positions 9 and 10 belongs to a further ring system and thus forms a spiro linkage point.

Photochromic spirodihydrophenanthropyrans

A photochromic plastic object which is composed of a transparent polymeric synthetic resin material, into or onto which at least one substantially mesoporous inorganic host structure is introduced or applied containing one or more embedded organic photochromic dye molecules so as to form a photochromic nanocomposite material. In contrast to prior techniques of adding or applying the photochromic organic dyes to the monomer mixture or prepolymer of a transparent synthetic resin material in a molecular form, in the photochromic plastic article of the present invention color is generated by using the photochromic nanocomposite particles or photochromic nanocomposite structures.

Photochromic plastic object

The present invention relates to photochromic benzopyrans and to the use thereof in plastics of all kinds, especially for ophthalmic purposes. The inventive compounds are photochromic benzopyran compounds in which a polycyclic aromatic is joined to the 5 and 6 positions of a benzopyran, where the bond in the 6 position is direct and the bond in the 5 position is via a mono- or diatomic bridge.

Photochromic benzopyrans

Photochromic h-annellated benzo[f]chromene compounds, especially photochromic compounds derived from benzo[f]chromenes, which compounds have particular long wavelength absorption maxima in their closed form and exhibit good performance in the open, colored form, so that good compatibility is achieved with indenonaphthopyrans which are diffused in phototropic glasses used in phototropic glass applications, and the use of such photochromic h-annellated benzo[f]chromene compounds in photochromic synthetic resin articles, particularly ophthalmic lenses.

Photochromic h-annellated benzo[f]chromene compounds

The present invention relates to photochromic 2H-naphtho[1,2-b]pyrans as well as their use in synthetic resins of all types, especially for ophthalmic purposes. In particular, the present invention relates to photochromic naphthopyran compounds, for which a further ring system is bonded to the f side of the naphthopyran. The inventive photochromic dyes generally have the general formula (I) wherein n, R, R, R, X, B and B' are defined as in claim. The inventive compounds are distinguished by good darkening and decolorizing properties and a very good service life.

Photochromic naphthopyrans

Photochromic 3H-naphtho[2,1-b]pyran compounds corresponding to formula I in which the groups Rto Rand B' have defined meanings and the use of such photochromic compounds in synthetic resin articles of all types, particularly for ophthalmic purposes. The photochromic 3H-naphtho[2,1-b]pyran derivatives have particularly long-waved absorption maxima in the open form, and when used in photochromic eyeglass lenses, produce essentially blue color tones which have a high darkening capacity.

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Munich, Germany

Udo Weigand