Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 1972, 37, 1520-1532
https://doi.org/10.1135/cccc19721520

Organic light-sensitive compounds. III. Pyrylium salt sensitizers in light-sensitive polymers

A. Mistr, M. Vávra, J. Skoupý and R. Zahradník

Crossref Cited-by Linking

  • Burov A. M., Pchelintseva N. V., Fedotova O. V.: Electronic absorption spectra of pyrylium and benzodihydrochromenylium salts. Chem Heterocycl Comp 2008, 44, 924. <https://doi.org/10.1007/s10593-008-0134-1>
  • Zimmermann Thomas, Krautscheid Harald: Ring transformations of heterocyclic compounds. XXV. Phenanthrene aldehyde imines via ring transformation of pyrylium salts with methylenedihydroisoquinolines—A novel access to the phenanthrene skeleton. Journal of Heterocyclic Chem 2007, 44, 1029. <https://doi.org/10.1002/jhet.5570440509>
  • Zimmermann Thomas: Ring transformations of heterocyclic compounds. XXIV. 1′,2′,5′,6′‐Tetrahydro‐4′H‐spiro[cyclohexa‐2,4‐diene‐1,2′‐pyrrolo[3,2,1‐ij]quinoline] and 1,2,4,5,6,7‐hexahydrospiro[azepino[3,2,1‐hi]indole‐2,1′‐cyclohexa[2,4]diene] – Two new spiro[cyclohexadiene‐azaheterocycles] easily accessible by pyrylium ring transformation. Journal of Heterocyclic Chem 2004, 41, 691. <https://doi.org/10.1002/jhet.5570410506>
  • Zimmermann Thomas, Brede Ortwin: Ring transformations of heterocyclic compounds. XXIII. The UV irradiation product of photochromic 2,4,6‐triaryl‐1‐(spiro[2H‐l‐benzopyran‐2,2′‐indoline]‐6‐yl)pyridinium salts ‐ A phenolate betaine or a pyridinium substituted merocyanine dye?. Journal of Heterocyclic Chem 2003, 40, 611. <https://doi.org/10.1002/jhet.5570400409>
  • Zimmermann Thomas: Ring transformations of heterocyclic compounds. XXI. Diastereoselective built‐up of an aroylcyclohexadiene moiety as second spiro‐connected ring at spiroindolines by pyrylium ring transformation. Journal of Heterocyclic Chem 2002, 39, 255. <https://doi.org/10.1002/jhet.5570390202>
  • Zimmermann Thomas, Hennig Lothar: Ring transformations of heterocyclic compounds. XXII. Pyrido[1,2‐a]indolium salts from 2‐methyl‐3H‐indoles by pyrylium mediated three carbon annelation. Journal of Heterocyclic Chem 2002, 39, 263. <https://doi.org/10.1002/jhet.5570390203>
  • Zimmermann Thomas: Ring transformations of heterocyclic compounds. XX Benzo‐fused spiro[cyclohexadiene‐dihydroindoles] by ring transformation of pyrylium salts with anhydrobases of benzo[e]‐ and benzo[g]indolium salts. Journal of Heterocyclic Chem 2000, 37, 885. <https://doi.org/10.1002/jhet.5570370435>
  • Zimmermann Thomas: Ring transformations of heterocyclic compounds. XVII, 2‐(2,4,6‐Triarylphenyl) substituted dihydro‐1H‐imidazolium, dihydrothiazolium and thiazolium salts from 2‐methyl derivatives by pyrylium and thiopyrylium ring transformations. Journal of Heterocyclic Chem 1999, 36, 813. <https://doi.org/10.1002/jhet.5570360339>
  • Zimmermann Thomas, Abram Ulrich: Ring transformations of heterocyclic compounds. XVIII . Spiro[cyclohexadiene‐indolines] with three stereocenters from pyrylium salts and chiral methyleneindolines — an example of a high diastereoselective ring transformation. Journal of Heterocyclic Chem 1999, 36, 1223. <https://doi.org/10.1002/jhet.5570360518>
  • Zimmermann Thomas, Abram Ulrich, Schmidt Klaus: Ring transformations of heterocyclic compounds. XVI. Spiro[cyclohexadiene‐dihydroacridines]. A novel class of spirodihydroacridines by ring transformation of pyrylium salts with 9‐methylacridine and its quaternary salts. Journal of Heterocyclic Chem 1998, 35, 787. <https://doi.org/10.1002/jhet.5570350403>
  • Galindo Francisco, Miranda Miguel A.: Pyrylium and thiopyrylium salts as electron transfer photosensitizers for the [27π+27π] cyclodimerization of poly (vinyl cinnamate) in solution. Journal of Photochemistry and Photobiology A: Chemistry 1998, 113, 155. <https://doi.org/10.1016/S1010-6030(97)00330-4>
  • Jayanthi S. S., Ramamurthy P.: Excited Singlet State Reactions of Thiopyrylium with Electron Donors:  Electron Transfer, Induction of Triplet by Internal and External Heavy Atom Effect, and Comparison of Pyrylium and Thiopyrylium Reactions. J. Phys. Chem. A 1998, 102, 511. <https://doi.org/10.1021/jp9701101>
  • Manoj N., Gopidas K.R.: Structure-photophysics correlation in a series of 2,6-dimethyl-4-arylpyrylium derivatives. Chemical Physics Letters 1997, 267, 567. <https://doi.org/10.1016/S0009-2614(97)00140-1>
  • Manoj N., Ajit Kumar R., Gopidas K.R.: Photophysical and electron transfer studies of a few 2,6-dimethyl-4-(alkylphenyl)pyrylium and thiopyrylium derivatives. Journal of Photochemistry and Photobiology A: Chemistry 1997, 109, 109. <https://doi.org/10.1016/S1010-6030(97)00112-3>
  • Zimmermann Thomas, Schmidt Klaus: Ring transformations of heterocyclic compounds. XIII. Bis(2,4,6‐triarylphenyl) substituted bispyridinium salts from methyl derivatives by double pyrylium and thiopyrylium ring transformations. Journal of Heterocyclic Chem 1996, 33, 783. <https://doi.org/10.1002/jhet.5570330342>
  • Zimmermann Thomas, Abram Ulrich, Schmidt Klaus: Ring transformations of heterocyclic compounds. XV. N‐(2‐hydroxyphenyl) substituted 2‐alkylamino‐4,6‐diarylbenzophenones by ring transformation of 2,4,6‐triarylpyrylium salts with anhydrobases of benzoxazolium salts. Journal of Heterocyclic Chem 1996, 33, 1679. <https://doi.org/10.1002/jhet.5570330621>
  • Zimmermann Thomas, Schmidt Klaus: Ring transformations of heterocyclic compounds. XIV. Ring transformations of pyrylium and thiopyrylium salts with anhydro‐bases derived from 1H‐benzimidazolium and benzothiazolium salts: An easy access to 2‐(2,4,6‐triarylphenyl) 1H‐benzimidazolium and benzothiazolium derivatives. Journal of Heterocyclic Chem 1996, 33, 1717. <https://doi.org/10.1002/jhet.5570330628>
  • Zimmermann Thomas: Ring transformations of heterocyclic compounds. X. A simple method for the conversion of methyl substituted pyridinium salts into 2,4,6‐triarylphenyl derivatives: The first (thio)pyrylium ring transformations with heterocyclic anhydrobases as carbon nucleophiles. Journal of Heterocyclic Chem 1995, 32, 563. <https://doi.org/10.1002/jhet.5570320232>
  • Zimmermann Thomas: Ring transformations of heterocyclic compounds. XI. 2,4,6‐triarylphenylquinolinium salts from methyl substituted derivatives via (thio)pyrylium ring transformations. Journal of Heterocyclic Chem 1995, 32, 991. <https://doi.org/10.1002/jhet.5570320353>
  • Zimmermann T., Pink Maren: Ringtransformationen heterocyclischer Verbindungen. XII. Neuartige Spiroindoline via Ringtransformation von 2,4,6-Triaryl-pyryliumsalzen mit 2-Methylen-indolinen. J. Prakt. Chem. 1995, 337, 368. <https://doi.org/10.1002/prac.19953370179>
  • Zimmermann Thomas: Ring transformations of heterocyclic compounds. IX. Trifluoromethyl Substituted 2‐Amino‐3,4,6‐triarylbenzophenones by Ring Transformation of 2,4,6‐Triarylpyrylium Salts with Trifluoromethylbenzyl Cyanides. Journal of Heterocyclic Chem 1994, 31, 277. <https://doi.org/10.1002/jhet.5570310203>
  • Zimmermann T.: Ringtransformationen heterocyclischer Verbindungen. VII. 2,4,5-Triaryl-benzophenone aus 2,4,6-Triaryl-pyryliumsalzen und Arylacetaldehyden: Erste Pyryliumringtransformationen mit Aldehyden als Kohlenstoffnucleophile. J. Prakt. Chem. 1994, 336, 303. <https://doi.org/10.1002/prac.19943360405>
  • Zimmermann Thomas, Pink Maren: Ringtransformationen heterocyclischer Verbindungen, VI. 3‐Nitrobenzonitrile aus 2,4,6‐Triarylpyryliumsalzen und Nitroacetonitril. Liebigs Ann. Chem. 1993, 1993, 1145. <https://doi.org/10.1002/jlac.1993199301183>
  • Zimmermann T.: Ringtransformationen heterocyclischer Verbindungen. IV [1] 3-Pyridylsubstituierte 2-Amino-benzophenone durch Ringtransformation von 2,4,6-Triaryl-pyryliumsalzen mit Pyridylacetonitrilen. J. Prakt. Chem. 1993, 335, 644. <https://doi.org/10.1002/prac.19933350713>
  • Zimmermann T.: Ringtransformationen heterocyclischer Verbindungen. V. [1] Pyrido[1,2-a]benzimidazol-4-carbonitrile via Ringtransformation von 2,4,6-Triaryl-pyryliumsalzen mit Benzimidazol-2-yl-acetonitril. J. Prakt. Chem. 1993, 335, 717. <https://doi.org/10.1002/prac.19933350814>
  • Zimmermann T., Fischer G. W., Olk B.: Pyryliumverbindungen. 45 [1]. 4‐Aroyl‐fluorene aus 2,4,6‐Triaryl‐pyryliumsalzen und Indan‐1‐on via 2‐(5‐Oxo‐pent‐2‐en‐1‐yliden)‐indan‐1‐one. J. Prakt. Chem. 1991, 333, 717. <https://doi.org/10.1002/prac.19913330506>
  • Zimmermann T., Fischer G. W., Olk B.: Pyryliumverbindungen. 46. 4‐Aroyl‐fluoren‐9‐one durch Ringtransformation von 2,4,6‐Triaryl‐pyryliumsalzen mit Indan‐1,3‐dion. J. Prakt. Chem. 1991, 333, 727. <https://doi.org/10.1002/prac.19913330507>
  • Zimmermann T., Fischer G. W., Kutschabsky L.: Pyryliumverbindungen. 41. 7aH‐Cyclopenta[b]pyran‐7‐one durch Ringtransformation von 2,4,6‐Triaryl‐pyryliumsalzen mit acyclischen 1,2‐Diketonen. J. Prakt. Chem. 1989, 331, 293. <https://doi.org/10.1002/prac.19893310216>
  • Zimmermann T., Fischer G. W., Olk B., Findeisen M.: Pyryliumverbindungen. 42. Benzocycloalkenone und Dihydro‐2H,7H‐1‐benzopyranone aus 2,4,6‐Triaryl‐pyryliumsalzen und Cycloalkan‐1,2‐dionen. J. Prakt. Chem. 1989, 331, 306. <https://doi.org/10.1002/prac.19893310217>
  • Zimmermann T., Fischer G. W., Teller J., Dehne H., Olk B.: Pyryliumverbindungen. 43 [1]. Arylsubstituierte 5‐(2‐Dialkylamino‐thiazol‐5‐yl)‐pentadienone aus 2,4,6‐Triaryl‐pyryliumsalzen und 2‐Dialkylamino‐4‐arylthiazolen. J. Prakt. Chem. 1989, 331, 843. <https://doi.org/10.1002/prac.19893310519>
  • Zimmermann T., Fischer G. W., Olk B.: Pyryliumverbindungen. 44 [1]. 2‐(2‐Hydroxy‐3‐oxo‐cycloalk‐1‐enyl)‐2H‐thiopyrane aus 2,4,6‐Triaryl‐thiopyryliumsalzen und Cycloalkan‐1,2‐dionen. J. Prakt. Chem. 1989, 331, 853. <https://doi.org/10.1002/prac.19893310520>
  • Zimmermann Thomas, Fischer Gerhard W.: Pyryliumverbindungen. 38. Zur Ringtransformation von 2,4,6‐Triaryl‐thiopyryliumsalzen mit Essigsäureanhydrid zu Arylbenzenen und Thiobenzophenonen. J. Prakt. Chem. 1988, 330, 35. <https://doi.org/10.1002/prac.19883300108>
  • Novikov V. N., Tymyanskii Ya. R., Feigel'man V. M., Knyazhanskii M. I.: Synthesis and spectral properties of furyl-substituted pyridines and pyrylium and pyridinium salts. Chem Heterocycl Compd 1988, 24, 1091. <https://doi.org/10.1007/BF00475680>
  • Knyazhanskii M. I., Tymyanskii Ya. R., Feigel'man V. M.: On the paper by A. F. Korunova, I. P. Krainov, and E. G. Protsenko, ?Electronic structure and spectral luminescent properties of 1,2,4,6-tetrasubstituted pyridinium salts?. Theor Exp Chem 1988, 23, 478. <https://doi.org/10.1007/BF00536375>
  • Zimmermann Thomas, Fischer Gerhard W.: Pyryliumverbindungen. 36. Substituierte Benzoesäureester aus 2,4,6‐Triaryl‐pyryliumsalzen und α‐Ketocarbonsäureestern. J. Prakt. Chem. 1987, 329, 499. <https://doi.org/10.1002/prac.19873290317>
  • Zimmermann Thomas, Fischer Gerhard W.: Pyryliumverbindungen. 37. Arylbenzene aus 2,4,6‐Triaryl‐pyryliumsalzen und Carbonsäureanhydriden. J. Prakt. Chem. 1987, 329, 975. <https://doi.org/10.1002/prac.19873290605>
  • Zimmermann Thomas, Fischer Gerhard W.: Pyryliumverbindungen. 32 [1]. 2‐Methoxy‐2H‐thiopyrane aus 2,4,6‐Triaryl‐thiopyryliumsalzen. J. Prakt. Chem. 1986, 328, 373. <https://doi.org/10.1002/prac.19863280311>
  • Zimmermann Thomas, Fischer Gerhard W.: Pyryliumverbindungen. 33 [1] 2‐Dialkylamino‐2H‐thiopyrane aus 2,4,6‐Triaryl‐thiopyryliumsalzen. J. Prakt. Chem. 1986, 328, 567. <https://doi.org/10.1002/prac.19863280416>
  • Zimmermann Thomas, Fischer Gerhard W.: Pyryliumverbindungen. 34 [1] 2‐Acetonyl‐2H‐thiopyrane aus 2,4,6‐Triaryl‐thiopyryliumsalzen. J. Prakt. Chem. 1986, 328, 573. <https://doi.org/10.1002/prac.19863280417>
  • Ten G. N., Kovalev I. F., Bazov V. P., Kharchenko V. G.: Spectral-luminescent properties of certain pyrylium and thiopyrylium salts. J Appl Spectrosc 1986, 45, 949. <https://doi.org/10.1007/BF00663518>
  • Fischer Gerhard W., Zimmermann Thomas: Pyrylium Compounds. XXVI. Comparative U.V./Vis. Studies on 3‐Methyl‐2,4,6‐triarylpyrylium Perchlorates. J. Prakt. Chem. 1985, 327, 151. <https://doi.org/10.1002/prac.19853270122>
  • Zimmermann Thomas, Fischer Gerhard W.: Pyryliumverbindungen. XXIX [1] Substituierte Benzophenone aus 2,4,6‐Triaryl‐pyryliumsalzen und Methyl(en)ketonen. J. Prakt. Chem. 1985, 327, 775. <https://doi.org/10.1002/prac.19853270510>
  • Klimenko S. K., Evtushenko I. Ya., Pronin A. F., Stolbova T. V., Kharchenko V. G.: Electronic spectra of 5,6-polymethylenethiapyrylium salts and certain oxygen analogs. Chem Heterocycl Compd 1985, 21, 161. <https://doi.org/10.1007/BF00504200>
  • Pozharskii A. F.: Heteroaromaticity (review). Chem Heterocycl Compd 1985, 21, 717. <https://doi.org/10.1007/BF00519137>
  • Tymyanskii Ya. R., Knyazhanskii M. I., Feigel'man V. M., Kharlanov V. A.: Molecular-structural aspects of formulation of spectral-luminescence properties of aryl-substituted pyridinium cations. J Appl Spectrosc 1985, 42, 394. <https://doi.org/10.1007/BF00662500>
  • Katritzky A. R., Agha B., de Ville G. Z., Lunt E., Knyazhanskii M. I., Tymyanskii Ya. R., Pyshchev A. I.: Photocyclization of 1,2-diaryl- and photobicyclization of 1,2,6-triarylpyridinium cations. Chem Heterocycl Compd 1984, 20, 1245. <https://doi.org/10.1007/BF00505716>
  • Fischer Gerhard W., Zimmermann Thomas: Isolierbare 2‐Dialkylamino‐2H‐thiopyrane aus 2,4,6‐Triaryl‐thiopyryliumsalzen. Zeitschrift fuer Chemie 1983, 23, 144. <https://doi.org/10.1002/zfch.19830230413>
  • Zvezdina �. A., Zhdanova M. P., Giryavenko I. I.: Reactions of heterocyclic cations with N-containing nucleophiles. 14. Recyclization of 2,6-diphenylpyrylium perchlorate under the influence of nucleophiles with an N-C-N fragment. Chem Heterocycl Compd 1983, 19, 714. <https://doi.org/10.1007/BF00506090>
  • Knyazhanskii M. I., Karmazin V. P., Olekhnovich E. P., Dorofeenko G. N.: Spectral luminescence properties caused by hyperconjugation in the 2-methylchromylium cation. J Appl Spectrosc 1975, 23, 1123. <https://doi.org/10.1007/BF00611762>
  • Karmazin V. P., Knyazhanskii M. I., Olekhnovich E. P., Dorofeenko G. N.: Spectral luminescence properties of some pyrylium salts. J Appl Spectrosc 1975, 22, 173. <https://doi.org/10.1007/BF00614252>
  • Zvezdina �. A., Zhdanova M. P., Bren' V. A., Dorofeenko G. N.: Reaction of 2,4,6-trimethyl- and 2,4,6-triphenylpyrylium perchlorates with heterocyclic amines. Chem Heterocycl Compd 1974, 10, 1285. <https://doi.org/10.1007/BF01175079>
  • MISTR A., VAVRA M., SKOUPY J., ZAHRADNIK R.: ChemInform Abstract: LICHTEMPFINDLICHE ORGANISCHE VERBINDUNGEN 3. MITT. PYRYLIUMSALZE ALS SENSIBILISATOREN IN LICHTEMPFINDLICHEN POLYMEREN. Chemischer Informationsdienst 1972, 3. <https://doi.org/10.1002/chin.197234283>