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S  TԣKK #" ``2h  ^*B QQ CC  T৘KK #" ``>~42h   `*B QQ CC  TKK #" ``%9K2h  `*B QQ CCz  NA [ ?texture_mid#" @@ +T3f3f80___PPT10. ` Textured : 0 '(    TKK #" `IV6  T Click to edit Master title style! !  NPKK ">< CjW  W#Click to edit Master subtitle style$ $  TKK #" ``2h  ^*B QQ CC  T KK #" ``>~42h   `*B QQ CC  TKK #" ``%9K2h  `*B QQ CCz  NA [ ?texture_mid#" @@ +T3f3f80___PPT10. `=; 0L0 << -,  <(    <8'A PIntramolecular photocyclization of new dithiophene-substituted o-divinylbenzenes>Q ?HHHh            <A i??"`  i>  <|? Jw 0D.Vidakovi 1), K. Mol anov 2), B. Koji-Prodi 2), M. `indler-Kulyk 1) 1)Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Maruliev trg 19, 10 000 Zagreb, Croatia 2)Laboratory for Chemical and Biological Crystallography, Department of Physical Chemistry, The Ruer Boakovi Institute, Bijeni ka cesta 54, 10 000 Zagreb,Croatia dragana.vidakovic@fkit.hr  ((((((((($$$$           i      `                 <JqL `Thiophenes and their polycyclic derivatives represent a class of important and well-studied heterocycles [1]. The interest in this kind of compounds has spread from early dye chemistry to modern drug design and self-assembled superstructures. Unsaturated thiophene derivatives show a versatile photoreactivity and formations of various photoproducts with remarkable electrochemical, optical, physical and biological properties [1]. $$$h  R        |   <|b M *In aim to investigate the effect of sulphur moiety on photobehaviour of dithiophene-substituted o-divinylbenzenes, the novel 2,2'-(1,2-phenylenedivinylene)dithiophene (3), 2,2'-(1,2-phenylenedivinylene)-5,5'-dimethyldithiophene (4) and 2,2'-(1,2-phenylenedivinylene)-5,5'-dibromodithiophene (5) were prepared, and compared with previously investigated difuro-substituted o-divinylbenzenes [2]. `$$G$$<$$>$$N$$$6        7 <  8          X   <~'FL1 >Contrary to these results, novel thiophene analogs 3-5 upon irradiation gave completely different photoproducts, the only observed products were dihydronaphtalenes (6-8), with traces of cyclophane (9). Formation of dihydronaphtalenes 6-8 could be explained by [1,6] electrocyclization and subsequent 1,5-H shift (scheme 2). According to this mechanism, replacement the furan moiety with thiophene, which is more aromatic than furan, may have influence on the excited state properties of this new hexatriene system and as concequence the formation of diverse photoproducts . ?3$$$$o$$$$$$$$$$$$<$$$j                             ,      " R8 tkR '16Z  ZeeA  ??"`80?  V@ tkR >tkR@ O O  ZeeA  ??"`Y/    ZeeA ??"`@O L  H0ee"`"h #  cis,cis-3aP 0@ 4  Hee"`b3 b4  cis,trans-3bP 0&  B  Hțee"`UCJ UD trans,trans-3cP02 t  6ĢPtkR JFig. 1 Photoisomerization of 2,2'-(1,2-phenylenedivinylene)dithiophene (3)8K D`+  r  s *@A? C"`kUCtKa P  <,\u7` [1] E. Campaigne, Thiophenes and their Benzo Derivatives: (iii) Synthesis and Applications in A.R. Katritzky (ed) Comprehensive Heterocyclic Chemistry; vol. 4, Part 3, Pergamon Press, Oxford 1984., 863-934. [2] I. `kori, N. Basari, }. Marini, A. Vianjevac, B. Koji-Prodi and M. `indler, Chem. Eur. J. 2005, 11, 543-551.G r $   !  c       d         7   <                       s JA   f&logo1CECP 2006"`cf  0 ! 6bf6/g ?a"Central European Conference on Photochemistry" 10th-14th February, 2008 Bad Hofgastein, Austria<b 1$$$~0   ' s PA $ f&pic_badhofgastein"`bBzK$g  08 E=AT NKjCZj  S ,A plakat"`|/E=ARp  S 2A ORTEP002b"`E,S  B S<:T &<Fig. 2 Molecular structure of photoproduct 6 (ORTEP diagram)<= 5      0Av&% *In the case of 2,2'-(1,2-phenylenedivinylene)difuran (1), during irradiation intermolecular [2+2] cycloaddition and intramolecular photocyloaddition took place to give bicyclo[3.2.1.]octadiene (2) and cyclobutane products, respectively [2].V 6$$$$.$         8 p207I 530I* ( H "`G$7I Sheme 2 Photoreactivity of 3-5, .  BA ?? "`p20XG 8 3-JkD 2s4JaI( ) <3BKHkD bFig. 3 1H NMR spectra (in CDCl3) of the aliphatic region of three new dihydronaphtalenes (6, 7, 8)pc D    n@ 3-JA 3-JAZ@ 3-J22 3-J22z 4 <A?"`3?.J22  6A s?"`X8-m:/ sZ@ 3>JA 3>JAz 5 <A? 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Jw 0D.Vidakovi 1), K. Mol anov 2), B. Koji-Prodi 2), M. `indler-Kulyk 1) 1)Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Maruliev trg 19, 10 000 Zagreb, Croatia 2)Laboratory for Chemical and Biological Crystallography, Department of Physical Chemistry, The Ruer Boakovi Institute, Bijeni ka cesta 54, 10 000 Zagreb,Croatia dragana.vidakovic@fkit.hr  ((((((((($$$$           i      `                 <JqL `Thiophenes and their polycyclic derivatives represent a class of important and well-studied heterocycles [1]. The interest in this kind of compounds has spread from early dye chemistry to modern drug design and self-assembled superstructures. Unsaturated thiophene derivatives show a versatile photoreactivity and formations of various photoproducts with remarkable electrochemical, optical, physical and biological properties [1]. $$$h  R        |   <|b M *In aim to investigate the effect of sulphur moiety on photobehaviour of dithiophene-substituted o-divinylbenzenes, the novel 2,2'-(1,2-phenylenedivinylene)dithiophene (3), 2,2'-(1,2-phenylenedivinylene)-5,5'-dimethyldithiophene (4) and 2,2'-(1,2-phenylenedivinylene)-5,5'-dibromodithiophene (5) were prepared, and compared with previously investigated difuro-substituted o-divinylbenzenes [2]. `$$G$$<$$>$$N$$$6        7 <  8          X   <~'FL1 >Contrary to these results, novel thiophene analogs 3-5 upon irradiation gave completely different photoproducts, the only observed products were dihydronaphtalenes (6-8), with traces of cyclophane (9). Formation of dihydronaphtalenes 6-8 could be explained by [1,6] electrocyclization and subsequent 1,5-H shift (scheme 2). According to this mechanism, replacement the furan moiety with thiophene, which is more aromatic than furan, may have influence on the excited state properties of this new hexatriene system and as concequence the formation of diverse photoproducts . ?3$$$$o$$$$$$$$$$$$<$$$j                             ,      " R8 tkR '16Z  ZeeA  ??"`80?  V@ tkR >tkR@ O O  ZeeA  ??"`Y/    ZeeA ??"`@O L  H0ee"`"h #  cis,cis-3aP 0@ 4  Hee"`b3 b4  cis,trans-3bP 0&  B  Hțee"`UCJ UD trans,trans-3cP02 t  6ĢPtkR JFig. 1 Photoisomerization of 2,2'-(1,2-phenylenedivinylene)dithiophene (3)8K D`+  r  s *@A? C"`kUCtKa P  <,\u7` [1] E. Campaigne, Thiophenes and their Benzo Derivatives: (iii) Synthesis and Applications in A.R. Katritzky (ed) Comprehensive Heterocyclic Chemistry; vol. 4, Part 3, Pergamon Press, Oxford 1984., 863-934. [2] I. `kori, N. Basari, }. Marini, A. Vianjevac, B. Koji-Prodi and M. `indler, Chem. Eur. 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Jw 0D.Vidakovi 1), K. Mol anov 2), B. Koji-Prodi 2), M. `indler-Kulyk 1) 1)Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Maruliev trg 19, 10 000 Zagreb, Croatia 2)Laboratory for Chemical and Biological Crystallography, Department of Physical Chemistry, The Ruer Boakovi Institute, Bijeni ka cesta 54, 10 000 Zagreb,Croatia dragana.vidakovic@fkit.hr  ((((((((($$$$           i      `                 <JqL `Thiophenes and their polycyclic derivatives represent a class of important and well-studied heterocycles [1]. The interest in this kind of compounds has spread from early dye chemistry to modern drug design and self-assembled superstructures. Unsaturated thiophene derivatives show a versatile photoreactivity and formations of various photoproducts with remarkable electrochemical, optical, physical and biological properties [1]. $$$h  R        |   <|b M *In aim to investigate the effect of sulphur moiety on photobehaviour of dithiophene-substituted o-divinylbenzenes, the novel 2,2'-(1,2-phenylenedivinylene)dithiophene (3), 2,2'-(1,2-phenylenedivinylene)-5,5'-dimethyldithiophene (4) and 2,2'-(1,2-phenylenedivinylene)-5,5'-dibromodithiophene (5) were prepared, and compared with previously investigated difuro-substituted o-divinylbenzenes [2]. `$$G$$<$$>$$N$$$6        7 <  8          [   <'FL1 AContrary to these results, novel thiophene analogs 3-5 upon irradiation gave completely different photoproducts, the only observed products were dihydronaphtalenes (6-8), with traces of cyclophane (9). Formation of dihydronaphtalenes 6-8 could be explained by [1,6] electrocyclization and subsequent 1,5-H shift (scheme 2). According to this mechanism, replacement of the furan moiety with thiophene, which is more aromatic than furan, may have influence on the excited state properties of this new hexatriene system and as concequence the formation of diverse photoproducts . B3$$$$o$$$$$$$$$$$$<$$$j                             ,      " R8 tkR '16Z  ZeeA  ??"`80?  V@ tkR >tkR@ O O  ZeeA  ??"`Y/    ZeeA ??"`@O L  Hpee"`"h #  cis,cis-3aP 0@ 4  Hee"`b3 b4  cis,trans-3bP 0&  B  Hee"`UCJ UD trans,trans-3cP02 t  6PtkR JFig. 1 Photoisomerization of 2,2'-(1,2-phenylenedivinylene)dithiophene (3)8K D`+  r  s *@A? C"`kUCtKa P  < \u7` [1] E. Campaigne, Thiophenes and their Benzo Derivatives: (iii) Synthesis and Applications in A.R. Katritzky (ed) Comprehensive Heterocyclic Chemistry; vol. 4, Part 3, Pergamon Press, Oxford 1984., 863-934. [2] I. `kori, N. Basari, }. Marini, A. Vianjevac, B. Koji-Prodi and M. `indler, Chem. Eur. J. 2005, 11, 543-551.G r $   !  c       d         7   <                       s JA   f&logo1CECP 2006"`cf  0 ! 6bf6/g ?a"Central European Conference on Photochemistry" 10th-14th February, 2008 Bad Hofgastein, Austria<b 1$$$~0   ' s PA $ f&pic_badhofgastein"`bBzK$g  08 E=AT NKjCZj  S ,A plakat"`|/E=ARp  S 2A ORTEP002b"`E,S  B S<:T &<Fig. 2 Molecular structure of photoproduct 6 (ORTEP diagram)<= 5      0\v&% mIn the case of 2,2'-(1,2-phenylenedivinylene)difuran (1), during irradiation intramolecular [2+2] cycloaddition and intermolecular photocyloaddition took place to give bicyclo[3.2.1.]octadiene (2) and cyclobutane dimers as main products, respectively [2].V 6$$$$=$         8 s207I 030I* ( HH "`G$7I Sheme 2 Photoreactivity of 3-5, .  BA ?? "`s20;G 8 3-JkD 2s4JaI( ) < 3BKHkD bFig. 3 1H NMR spectra (in CDCl3) of the aliphatic region of three new dihydronaphtalenes (6, 7, 8)pc D    @ 3-JA 3-JA`@ 3-J22 3-J22z 4 <A?"`3?.J22  <A s??"`X8-m:/ s`@ 3>JA 3>JAz 5 <A? 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Mol anov 2), B. Koji-Prodi 2), M. `indler-Kulyk 1) 1)Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Maruliev trg 19, 10 000 Zagreb, Croatia 2)Laboratory for Chemical and Biological Crystallography, Department of Physical Chemistry, The Ruer Boakovi Institute, Bijeni ka cesta 54, 10 000 Zagreb,Croatia dragana.vidakovic@fkit.hr  ((((((((($$$$           i      `                 <qL `Thiophenes and their polycyclic derivatives represent a class of important and well-studied heterocycles [1]. The interest in this kind of compounds has spread from early dye chemistry to modern drug design and self-assembled superstructures. 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According to this mechanism, replacement of the furan moiety with thiophene, which is more aromatic than furan, may have influence on the excited state properties of this new hexatriene system and as concequence the formation of diverse photoproducts . B3$$$$o$$$$$$$$$$$$<$$$j                             ,      " S8 tkR '16Z  ZeeA  ??"`80?  W@ tkR >tkR@ O O  ZeeA  ??"`Y/    ZeeA ??"`@O L  H\ee"`"h #  cis,cis-3aP 0@ 4  Hee"`b3 b4  cis,trans-3bP 0&  B  Hee"`UCJ UD trans,trans-3cP02 u  6PtkR KFig. 1. Photoisomerization of 2,2'-(1,2-phenylenedivinylene)dithiophene (3)8L D`+  r  s *@A? C"`kUCtKa P  <\u7` [1] E. Campaigne, Thiophenes and their Benzo Derivatives: (iii) Synthesis and Applications in A.R. Katritzky (ed) Comprehensive Heterocyclic Chemistry; vol. 4, Part 3, Pergamon Press, Oxford 1984., 863-934. [2] I. `kori, N. Basari, }. Marini, A. Vianjevac, B. Koji-Prodi and M. `indler, Chem. Eur. J. 2005, 11, 543-551.G r $   !  c       d         7   <                       s JA   f&logo1CECP 2006"`cf  0 ! 6!bf6/g ?a"Central European Conference on Photochemistry" 10th-14th February, 2008 Bad Hofgastein, Austria<b 1$$$~0   ' s PA $ f&pic_badhofgastein"`bBzK$g  08 E=AT NKjCZj  S ,A plakat"`|/E=ARp  S 2A ORTEP002b"`E,S  B+ Sz:T '=Fig. 2. Molecular structure of photoproduct 6 (ORTEP diagram)<> 5      0>v&% mIn the case of 2,2'-(1,2-phenylenedivinylene)difuran (1), during irradiation intramolecular [2+2] cycloaddition and intermolecular photocyloaddition took place to give bicyclo[3.2.1.]octadiene (2) and cyclobutane dimers as main products, respectively [2].V 6$$$$=$         @@`` Z9**>> 5()      HH  8 s207I 030I+ ( HdK "`G3%7I Sheme 2. Photoreactivity of 3-5, .   BA ?? 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Mol anov 2), B. Koji-Prodi 2), M. `indler-Kulyk 1) 1)Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Maruliev trg 19, 10 000 Zagreb, Croatia 2)Laboratory for Chemical and Biological Crystallography, Department of Physical Chemistry, The Ruer Boakovi Institute, Bijeni ka cesta 54, 10 000 Zagreb,Croatia dragana.vidakovic@fkit.hr  ((((((((($$$$           i      `                 <qL `Thiophenes and their polycyclic derivatives represent a class of important and well-studied heterocycles [1]. The interest in this kind of compounds has spread from early dye chemistry to modern drug design and self-assembled superstructures. Unsaturated thiophene derivatives show a versatile photoreactivity and formations of various photoproducts with remarkable electrochemical, optical, physical and biological properties [1]. $$$h  R        |   <l M *In aim to investigate the effect of sulphur moiety on photobehaviour of dithiophene-substituted o-divinylbenzenes, the novel 2,2'-(1,2-phenylenedivinylene)dithiophene (3), 2,2'-(1,2-phenylenedivinylene)-5,5'-dimethyldithiophene (4) and 2,2'-(1,2-phenylenedivinylene)-5,5'-dibromodithiophene (5) were prepared, and compared with previously investigated difuro-substituted o-divinylbenzenes [2]. `$$G$$<$$>$$N$$$6        7 <  8          [   <Ȯ'FL1 AContrary to these results, novel thiophene analogs 3-5 upon irradiation gave completely different photoproducts, the only observed products were dihydronaphtalenes (6-8), with traces of cyclophane (9). Formation of dihydronaphtalenes 6-8 could be explained by [1,6] electrocyclization and subsequent 1,5-H shift (scheme 2). According to this mechanism, replacement of the furan moiety with thiophene, which is more aromatic than furan, may have influence on the excited state properties of this new hexatriene system and as concequence the formation of diverse photoproducts . B3$$$$o$$$$$$$$$$$$<$$$j                             ,      " G8 tkR '16Z  ZeeA  ??"`80?  K@ tkR >tkR@ O O  ZeeA  ??"`Y/    ZeeA ??"`@O L  H\ee"`"h #  cis,cis-3aP 0@ 4  Hee"`b3 b4  cis,trans-3bP 0&  B  Hee"`UCJ UD trans,trans-3cP02 i  6PtkR MFigure 1. Photoisomerization of 2,2'-(1,2-phenylenedivinylene)dithiophene (3)8N  DR +  r  s *@A? C"`kUCtKa P  <\u7` [1] E. Campaigne, Thiophenes and their Benzo Derivatives: (iii) Synthesis and Applications in A.R. Katritzky (ed) Comprehensive Heterocyclic Chemistry; vol. 4, Part 3, Pergamon Press, Oxford 1984., 863-934. [2] I. `kori, N. Basari, }. Marini, A. Vianjevac, B. Koji-Prodi and M. `indler, Chem. Eur. J. 2005, 11, 543-551.G r $   !  c       d         7   <                       s JA   f&logo1CECP 2006"`cf  0 ! 6!bf6/g ?a"Central European Conference on Photochemistry" 10th-14th February, 2008 Bad Hofgastein, Austria<b 1$$$~0   ' s PA $ f&pic_badhofgastein"`bBzK$g  08 E=AT NKjCZj  S ,A plakat"`|/E=ARp  S 2A ORTEP002b"`E,S  B+ S;T ?Figure 2. Molecular structure of photoproduct 6 (ORTEP diagram)<@  5|       0>v&% mIn the case of 2,2'-(1,2-phenylenedivinylene)difuran (1), during irradiation intramolecular [2+2] cycloaddition and intermolecular photocyloaddition took place to give bicyclo[3.2.1.]octadiene (2) and cyclobutane dimers as main products, respectively [2].V 6$$$$=$         8 s207I 030I+ ( HdK "`G3%7I Sheme 2. Photoreactivity of 3-5, .   BA ?? "`s20;G ,8 E42KnJ 2E4KnJH ) <PQ E4 GKnJ vFigure 3. 1H NMR spectra (in CDCl3. 300 and 600 Mhz) of the aliphatic region of three new dihydronaphtalenes (6, 7, 8)pw  U   T 3-JA #  42JwF`@ 3-J22 3-J22z 4 <A?"`3?.J22  <A s??"`X8-m:/ s`@ 3>JA 3>JAz 5 <A? "`3>JA  <A t??"`81>#;? t`@ 33J)= 33J)=z 6 <A ?"`33J)=  <A u??"`88^;L: u8 )G2' )G2'  <A ~??)G}% ~.  <`)%62' Scheme 1. Photoreactivity of 1<  <v  PA [ ?h_009a"@` 3380___PPT10.Y`Zrv v"19(OPj   i.CorelPhotoPaint.Image.8 .CorelPhotoPaint.Image.806Corel PHOTO-PAINT 8.0 Image  Graph Origin50.Graph0Origin Graph  Graph Origin50.Graph0Origin Graph  Graph Origin50.Graph0Origin Graphhome2.htmlVhttp://www.ptc.tugraz.at/gastein/home2.htmllhttp://www.hotel-tirol.at/images/pic_badhofgastein.jpglhttp://www.hotel-tirol.at/images/pic_badhofgastein.jpgs&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawingt&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawingu&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawing~&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawing&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawing/ 00DArialNew RomanTTqܖ 0ܖ"DTahomaew RomanTTqܖ 0ܖ" DWingdingsRomanTTqܖ 0ܖ0DTimes New RomanTTqܖ 0ܖ A .  @n?" dd@  @@`` Z9**>> 5()      HH,,HH@A   () 5 xR$.Kb|MR$@̘kh. ?M2$}(h2$^m%v p}CBPb$I=eJ|{X2$Џtݫ14p2$aD$)}#Aev"fXR$1h8O*YX-kR$t'Q^'a,Y(R$b~ K0@w ;2$Ul֝%|_(UR2$y1e7[t?$2$*|Ag:+J5RvR$W3VN::U5@'uT2$|7z` փP$$$$b$8#2| CQ2$mj*:t} $+$2$p[tͰvM 6$2$+&oɵ2 {Ү?8QC C 0AA f@8:;wNO ʚ;`8ʚ;g4dd 0Xp(5p'<4dddd w 0Tq<4!d!d w 0Tq 80___PPT10 pp`>; 0L0 f=^= -0  <(    <oKA PIntramolecular photocyclization of new dithiophene-substituted o-divinylbenzenes>Q ?HHHh            <A i??"`!   i>  <8Hw 0D.Vidakovi 1), K. Mol anov 2), B. Koji-Prodi 2), M. `indler-Kulyk 1) 1)Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Maruliev trg 19, 10 000 Zagreb, Croatia 2)Laboratory for Chemical and Biological Crystallography, Department of Physical Chemistry, The Ruer Boakovi Institute, Bijeni ka cesta 54, 10 000 Zagreb,Croatia dragana.vidakovic@fkit.hr  ((((((((($$$$           i      `                 <qL `Thiophenes and their polycyclic derivatives represent a class of important and well-studied heterocycles [1]. The interest in this kind of compounds has spread from early dye chemistry to modern drug design and self-assembled superstructures. Unsaturated thiophene derivatives show a versatile photoreactivity and formations of various photoproducts with remarkable electrochemical, optical, physical and biological properties [1]. $$$h  R        |   <l M *In aim to investigate the effect of sulphur moiety on photobehaviour of dithiophene-substituted o-divinylbenzenes, the novel 2,2'-(1,2-phenylenedivinylene)dithiophene (3), 2,2'-(1,2-phenylenedivinylene)-5,5'-dimethyldithiophene (4) and 2,2'-(1,2-phenylenedivinylene)-5,5'-dibromodithiophene (5) were prepared, and compared with previously investigated difuro-substituted o-divinylbenzenes [2]. `$$G$$<$$>$$N$$$6        7 <  8          [   <Ȯ'FL1 AContrary to these results, novel thiophene analogs 3-5 upon irradiation gave completely different photoproducts, the only observed products were dihydronaphtalenes (6-8), with traces of cyclophane (9). Formation of dihydronaphtalenes 6-8 could be explained by [1,6] electrocyclization and subsequent 1,5-H shift (scheme 2). According to this mechanism, replacement of the furan moiety with thiophene, which is more aromatic than furan, may have influence on the excited state properties of this new hexatriene system and as concequence the formation of diverse photoproducts . B3$$$$o$$$$$$$$$$$$<$$$j                             ,      " G8 tkR '16Z  ZeeA  ??"`80?  K@ tkR >tkR@ O O  ZeeA  ??"`Y/    ZeeA ??"`@O L  H\ee"`"h #  cis,cis-3aP 0@ 4  Hee"`b3 b4  cis,trans-3bP 0&  B  Hee"`UCJ UD trans,trans-3cP02 i  6PtkR MFigure 1. Photoisomerization of 2,2'-(1,2-phenylenedivinylene)dithiophene (3)8N  DR +  r  s *@A? C"`D M P  <\u7` [1] E. Campaigne, Thiophenes and their Benzo Derivatives: (iii) Synthesis and Applications in A.R. Katritzky (ed) Comprehensive Heterocyclic Chemistry; vol. 4, Part 3, Pergamon Press, Oxford 1984., 863-934. [2] I. `kori, N. Basari, }. Marini, A. Vianjevac, B. Koji-Prodi and M. `indler, Chem. Eur. J. 2005, 11, 543-551.G r $   !  c       d         7   <                       s JA   f&logo1CECP 2006"`d[ f  0 ! 6!bf6/g ?a"Central European Conference on Photochemistry" 10th-14th February, 2008 Bad Hofgastein, Austria<b 1$$$~0   ' s PA $ f&pic_badhofgastein"`b#CK$g  08 E=AT NKjCZj  S ,A plakat"`|/E=ARp  S 2A ORTEP002b"`E,S  B+ S;T ?Figure 2. Molecular structure of photoproduct 6 (ORTEP diagram)<@  5|       0>v&% mIn the case of 2,2'-(1,2-phenylenedivinylene)difuran (1), during irradiation intramolecular [2+2] cycloaddition and intermolecular photocyloaddition took place to give bicyclo[3.2.1.]octadiene (2) and cyclobutane dimers as main products, respectively [2].V 6$$$$=$         8 s207I 030I+ ( HdK "`G3%7I Sheme 2. Photoreactivity of 3-5, .   BA ?? "`s20;G ,8 E42KnJ 2E4KnJH ) <PQ E4 GKnJ vFigure 3. 1H NMR spectra (in CDCl3. 300 and 600 Mhz) of the aliphatic region of three new dihydronaphtalenes (6, 7, 8)pw  U   T 3-JA #  42JwF`@ 3-J22 3-J22z 4 <A?"`3?.J22  <A s??"`X8-m:/ s`@ 3>JA 3>JAz 5 <A? "`3>JA  <A t??"`81>#;? t`@ 33J)= 33J)=z 6 <A ?"`33J)=  <A u??"`88^;L: u8 )G2' )G2'  <A ~??)G}% ~.  <`)%62' Scheme 1. Photoreactivity of 1<  <v  PA [ ?h_009a"@` 3380___PPT10.Y`Zr^:11(igin50.Graph0Origin Graph  Graph Origin50.Graph0Origin Graph  Graph Origin50.Graph0Origin Graphhome2.htmlVhttp://www.ptc.tugraz.at/gastein/home2.htmllhttp://www.hotel-tirol.at/images/pic_badhofgastein.jpglhttp://www.hotel-tirol.at/images/pic_badhofgastein.jpgs&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawingt&CS ChemDraw Dr{awing *ChemDraw.Document.6.00&CS ChemDraw Drawingu&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawing~&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawing&CS ChemDraw Drawing *ChemDraw.Document.5.00&CS ChemDraw Drawing/ 00DArialNew L|0z[ 0DTahomaew L|0z[ 0" DWingdingsL|0z[ 00DTimes New Roman0z[ 0 A .  @n?" dd@  @@`` Z9**>> 5()    ,,HH@A   () 5 xR$.Kb|MR$@̘kh. ?M2$}(h2$^m%v p}CBPb$I=eJ|{X2$Џtݫ14p2$aD$)}#Aev"fXR$1h8O*YX-kR$t'Q^'a,Y(R$b~ K0@w ;2$Ul֝%|_(UR2$y1e7[t?$2$*|Ag:+J5RvR$W3VN::U5@'uT2$|7z` փP$$$$b$8#2| CQ2$mj*:t} $+$2$p[tͰvM 6$2$+&oɵ2 {Ү?8QC C 0AA f@8:;wNO ʚ;`8ʚ;g4!d!di 0  p(5p'<4dddd w 0T(,<4!d!d w 0T(, 80___PPT10 ppX  >; 0L0 f=^= -0  <(    <&KA PIntramolecular photocyclization of new dithiophene-substituted o-divinylbenzenes>Q ?HHHh            <A i??"`!   i>  <>Hw 0D.Vidakovi 1), K. Mol anov 2), B. Koji-Prodi 2), M. `indler-Kulyk 1) 1)Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Maruliev trg 19, 10 000 Zagreb, Croatia 2)Laboratory for Chemical and Biological Crystallography, Department of Physical Chemistry, The Ruer Boakovi Institute, Bijeni ka cesta 54, 10 000 Zagreb,Croatia dragana.vidakovic@fkit.hr  ((((((((($$$$           i      `                 <IqL `Thiophenes and their polycyclic derivatives represent a class of important and well-studied heterocycles [1]. The interest in this kind of compounds has spread from early dye chemistry to modern drug design and self-assembled superstructures. Unsaturated thiophene derivatives show a versatile photoreactivity and formations of various photoproducts with remarkable electrochemical, optical, physical and biological properties [1]. $$$h  R        |   <\a M *In aim to investigate the effect of sulphur moiety on photobehaviour of dithiophene-substituted o-divinylbenzenes, the novel 2,2'-(1,2-phenylenedivinylene)dithiophene (3), 2,2'-(1,2-phenylenedivinylene)-5,5'-dimethyldithiophene (4) and 2,2'-(1,2-phenylenedivinylene)-5,5'-dibromodithiophene (5) were prepared, and compared with previously investigated difuro-substituted o-divinylbenzenes [2]. `$$G$$<$$>$$N$$$6        7 <  8          [   <'FL1 AContrary to these results, novel thiophene analogs 3-5 upon irradiation gave completely different photoproducts, the only observed products were dihydronaphtalenes (6-8), with traces of cyclophane (9). Formation of dihydronaphtalenes 6-8 could be explained by [1,6] electrocyclization and subsequent 1,5-H shift (scheme 2). According to this mechanism, replacement of the furan moiety with thiophene, which is more aromatic than furan, may have influence on the excited state properties of this new hexatriene system and as concequence the formation of diverse photoproducts . B3$$$$o$$$$$$$$$$$$<$$$j                             ,      " G8 tkR '16Z  ZeeA  ??"`80?  K@ tkR >tkR@ O O  ZeeA  ??"`Y/    ZeeA ??"`@O L  Hnee"`"h #  cis,cis-3aP 0@ 4  H0ee"`b3 b4  cis,trans-3bP 0&  B  H4ee"`UCJ UD trans,trans-3cP02 i  68PtkR MFigure 1. Photoisomerization of 2,2'-(1,2-phenylenedivinylene)dithiophene (3)8N  DR +  r  s *@A? C"`D M P  <\u7` [1] E. Campaigne, Thiophenes and their Benzo Derivatives: (iii) Synthesis and Applications in A.R. Katritzky (ed) Comprehensive Heterocyclic Chemistry; vol. 4, Part 3, Pergamon Press, Oxford 1984., 863-934. [2] I. `kori, N. Basari, }. Marini, A. Vianjevac, B. Koji-Prodi and M. `indler, Chem. Eur. J. 2005, 11, 543-551.G r $   !  c       d         7   <                       s JA   f&logo1CECP 2006"`d[ f  0 ! 6bf6/g ?a"Central European Conference on Photochemistry" 10th-14th February, 2008 Bad Hofgastein, Austria<b 1$$$~0   ' s PA $ f&pic_badhofgastein"`b#CK$g  08 E=AT NKjCZj  S ,A plakat"`|/E=ARp  S 2A ORTEP002b"`E,S  B( S;T ?Figure 2. Molecular structure of photoproduct 6 (ORTEP diagram)<@  5|       0\v&% mIn the case of 2,2'-(1,2-phenylenedivinylene)difuran (1), during irradiation intramolecular [2+2] cycloaddition and intermolecular photocyloaddition took place to give bicyclo[3.2.1.]octadiene (2) and cyclobutane dimers as main products, respectively [2].V 6$$$$=$           HH,,HH@A   () 5 xR$.Kb|MR$@̘kh. ?8 s207I 030I+ ( H "`G3%7I Sheme 2. Photoreactivity of 3-5, .   BA ?? "`s20;G ,8 E42KnJ 2E4KnJH ) <  E4 GKnJ vFigure 3. 1H NMR spectra (in CDCl3. 300 and 600 MHz) of the aliphatic region of three new dihydronaphtalenes (6, 7, 8)pw  U   T 3-JA #  42JwF`@ 3-J22 3-J22z 4 <A?"`3?.J22  <A s??"`X8-m:/ s`@ 3>JA 3>JAz 5 <A? "`3>JA  <A t??"`81>#;? t`@ 33J)= 33J)=z 6 <A ?"`33J)=  <A u??"`88^;L: u8 )G2' )G2'  <A ~??)G}% ~.  <$)%62' Scheme 1. Photoreactivity of 1<  <v  PA [ ?h_009a"@` 3380___PPT10.Y`Zr*0@n11(OPj   i.CorelPhotoPaint.Image.8 .CorelPhotoPaint.Image.806Corel PHOTO-PAINT 8.0 Image  Graph Or  Graph Origin50.Graph0Origin Graph  Graph Origin50.Graph0Origin Graphhome2.htmlVhttp://www.ptc.tugraz.at/gastein/home2.htmllhttp://www.hotel-tirol.at/images/pic_badhofgastein.jpglhttp://www.hotel-tirol.at/images/pic_badhofgastein.jpgs&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawingt&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDr`      !"#$%&'()*+,-./0123456789:;<=>?@ABCDEFGHIJKLMNOPQRSTUVWXY[]^_}abcdefghijklmnopqrstuvwxyz{|~aw Drawingu&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawing~&CS ChemDraw Drawing *ChemDraw.Document.6.00&CS ChemDraw Drawing&CS ChemDraw Drawing *ChemDraw.Document.5.00&CS ChemDraw Drawing/ 00DArialNew RomanTT,ܖ 0ܖDTahomaew RomanTT,ܖ 0ܖ" DWingdingsRomanTT,ܖ 0ܖ0DTimes New RomanTT,ܖ 0ܖ A .  @n?" dd@  @@`` Z9**>> 5()      M2$}(h2$^m%v p}CBPb$I=eJ|{X2$Џtݫ14p2$aD$)}#Aev"fXR$1h8O*YX-kR$t'Q^'a,Y(R$b~ K0@w ;2$Ul֝%|_(UR2$y1e7[t?$2$*|Ag:+J5RvR$W3VN::U5@'uT2$|7z` փP$$$$b$8#2| CQ2$mj*:t} $+$2$p[tͰvM 6$2$+&oɵ2 {Ү?8QC C 0AA f@8:;wNO ʚ;`8ʚ;g4!d!d z[ 0 p(5p'<4ddddL 0$|<4!d!dL 0$| 80___PPT10 ppX  h>;K0 == -<  <(    <v<KA PIntramolecular photocyclization of new dithiophene-substituted o-divinylbenzenes>Q ?HHHh            <A i??"`!   i>  <<<Hw 0D.Vidakovi 1), K. Mol anov 2), B. Koji-Prodi 2), M. `indler-Kulyk 1) 1)Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Maruliev trg 19, 10 000 Zagreb, Croatia 2)Laboratory for Chemical and Biological Crystallography, Department of Physical Chemistry, The Ruer Boakovi Institute, Bijeni ka cesta 54, 10 000 Zagreb,Croatia dragana.vidakovic@fkit.hr  ((((((((($$$$           i      `                 <\<qL `Thiophenes and their polycyclic derivatives represent a class of important and well-studied heterocycles [1]. The interest in this kind of compounds has spread from early dye chemistry to modern drug design and self-assembled superstructures. Unsaturated thiophene derivatives show a versatile photoreactivity and formations of various photoproducts with remarkable electrochemical, optical, physical and biological properties [1]. $$$h  R        |   << L 6In aim to investigate the effect of sulphur moiety on photobehaviour of dithiophene-substituted o-divinylbenzenes, the novel 2,2'-(1,2-phenylenedivinylene)dithiophene (3), 2,2'-(1,2-phenylenedivinylene)-5,5'-dimethyldithiophene (4) and 2,2'-(1,2-phenylenedivinylene)-5,5'-dibromodithiophene (5) were prepared, and compared with previously investigated difuro-substituted o-divinylbenzenes [2]. `$$G$$<$$>$$N$$$6        7 <  8          g   <<<'FL1 AContrary to these results, novel thiophene analogs 3-5 upon irradiation gave completely different photoproducts, the only observed products were dihydronaphtalenes (6-8), with traces of cyclophane (9). Formation of dihydronaphtalenes 6-8 could be explained by [1,6] electrocyclization and subsequent 1,5-H shift (scheme 2). According to this mechanism, replacement of the furan moiety with thiophene, which is more aromatic than furan, may have influence on the excited state properties of this new hexatriene system and as concequence the formation of diverse photoproducts .,E3$$$$o$$$$$$$$$$$$<$$$j                             ,      " G8 tkR '16Z  ZeeA  ??"`80?  K@ tkR >tkR@ O O  ZeeA  ??"`Y/    ZeeA ??"`@O L  H4<ee"`"h #  cis,cis-3aP 0@ 4  H<ee"`b3 b4  cis,trans-3bP 0&  B  H<ee"`UCJ UD trans,trans-3cP02 i  6<PtkR MFigure 1. Photoisomerization of 2,2'-(1,2-phenylenedivinylene)dithiophene (3)8N  DR +  r  s *@A? C"`D M 6  <C\u7` [1] E. Campaigne, Thiophenes and their Benzo Derivatives: (iii) Synthesis and Applications in A.R. Katritzky (ed) Comprehensive Heterocyclic Chemistry; vol. 4, Part 3, Pergamon Press, Oxford 1984., 863-934. [2] I. `kori, N. Basari, }. Marini, A. Vianjevac, B. Koji-Prodi and M. `indler, Chem. Eur. J. 2005, 11, 543-551.G r $   !  c       J         7   <                    s JA   f&logo1CECP 2006"`d[ f U 0 ! 6Cbf6/g ?a"Central European Conference on Photochemistry" 10th-14th February, 2008 Bad Hofgastein, Austria<b 1$$$~0   ' s PA $ f&pic_badhofgastein"`b#CK$g U 08 <NKCG[ NK<CG[j  S ,A plakat"`B1NKCXp  S 2A ORTEP002b"`j|K.X  6TC <XBG[ uFigure 2. Molecular structure of photoproduct 6 (left) as determined by X-ray crstyallography. The molecules in crystals are disordered over two positions (right).>  p    u  0H+Cv&% oIn the case of 2,2'-(1,2-phenylenedivinylene)difuran (1), during irradiation intramolecular [2+2] cycloaddition and intermolecular photocyloaddition took place to give bicyclo[3.2.1.]octadiene (2) and cyclobutane dimers as main products, respectively [2].X 6$$$$=$         8 2 3J 2 3J+ ( HP3C"`gH$J Sheme 2. Photoreactivity of 3-5, .   BA ??"`2 3.I ,8 D40M.J 03M.JH ) <8CD4GM.J vFigure 3. 1H NMR spectra (in CDCl3. 300 and 600 MHz) of the aliphatic region of three new dihydronaphtalenes (6, 7, 8)pw  U   T 3-JA # 40M2G`@ 3-J22 3-J22z 4 <A?"`3?.J22  <A s??"`X8-m:/ s`@ 3>JA 3>JAz 5 <A? "`3>JA  <A t??"`81>#;? t`@ 33J)= 33J)=z 6 <A ?"`33J)=  <A u??"`88^;L: u8 )G' )H'  <A ~??)G}% ~.  <GC)%]6' Scheme 1. Photoreactivity of 1<  <v  PA [ ?h_009a"@` 3380___PPT10.Y`Zr|n? 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Mol anov 2), B. Koji-Prodi 2), M. `indler-Kulyk 1) 1)Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Maruliev trg 19, 10 000 Zagreb, Croatia 2)Laboratory for Chemical and Biological Crystallography, Department of Physical Chemistry, The Ruer Boakovi Institute, Bijeni ka cesta 54, 10 000 Zagreb,Croatia dragana.vidakovic@fkit.hr  ((((((((($$$$           i      `                 <\<qL `Thiophenes and their polycyclic derivatives represent a class of important and well-studied heterocycles [1]. The interest in this kind of compounds has spread from early dye chemistry to modern drug design and self-assembled superstructures. 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Formation of dihydronaphtalenes 6-8 could be explained by [1,6] electrocyclization and subsequent 1,5-H shift (scheme 2). According to this mechanism, replacement of the furan moiety with thiophene, which is more aromatic than furan, may have influence on the excited state properties of this new hexatriene system and as concequence the formation of diverse photoproducts .,E3$$$$o$$$$$$$$$$$$<$$$j                             ,      " G8 tkR '16Z  ZeeA  ??"`80?  K@ tkR >tkR@ O O  ZeeA  ??"`Y/    ZeeA ??"`@O L  H4<ee"`"h #  cis,cis-3aP 0@ 4  H<ee"`b3 b4  cis,trans-3bP 0&  B  H<ee"`UCJ UD trans,trans-3cP02 i  6<PtkR MFigure 1. Photoisomerization of 2,2'-(1,2-phenylenedivinylene)dithiophene (3)8N  DR +  6  <C\u7` [1] E. Campaigne, Thiophenes and their Benzo Derivatives: (iii) Synthesis and Applications in A.R. Katritzky (ed) Comprehensive Heterocyclic Chemistry; vol. 4, Part 3, Pergamon Press, Oxford 1984., 863-934. [2] I. `kori, N. Basari, }. Marini, A. Vianjevac, B. Koji-Prodi and M. `indler, Chem. Eur. J. 2005, 11, 543-551.G r $   !  c       J         7   <                    s JA   f&logo1CECP 2006"`d[ f U 0 ! 6Cbf6/g ?a"Central European Conference on Photochemistry" 10th-14th February, 2008 Bad Hofgastein, Austria<b 1$$$~0   ' s PA $ f&pic_badhofgastein"`b#CK$g U 08 <NKCG[ NK<CG[j  S ,A plakat"`B1NKCXp  S 2A ORTEP002b"`j|K.X  6TC <XBG[ uFigure 2. Molecular structure of photoproduct 6 (left) as determined by X-ray crstyallography. The molecules in crystals are disordered over two positions (right).>  p    u  0H+Cv&% oIn the case of 2,2'-(1,2-phenylenedivinylene)difuran (1), during irradiation intramolecular [2+2] cycloaddition and intermolecular photocyloaddition took place to give bicyclo[3.2.1.]octadiene (2) and cyclobutane dimers as main products, respectively [2].X 6$$$$=$         8 2 3J 2 3J+ ( HP3C"`gH$J Sheme 2. Photoreactivity of 3-5, .   BA ??"`2 3.I ,8 D40M.J 03M.JH ) <8CD4GM.J vFigure 3. 1H NMR spectra (in CDCl3. 300 and 600 MHz) of the aliphatic region of three new dihydronaphtalenes (6, 7, 8)pw  U   T 3-JA # 40M2G`@ 3-J22 3-J22z 4 <A?"`3?.J22  <A s??"`X8-m:/ s`@ 3>JA 3>JAz 5 <A? "`3>JA  <A t??"`81>#;? t`@ 33J)= 33J)=z 6 <A ?"`33J)=  <A u??"`88^;L: u8 )G' )H'  <A ~??)G}% ~.  <GC)%]6' Scheme 1. Photoreactivity of 1<  <R  C *A IRB-logoCL v  PA [ ?h_009a"@` 3380___PPT10.Y`Zra? =?1(OPj   i.CorelPhotoPaint.Image.8 .CorelPhotoPaint.Image.806Corel PHOTO-PAINT 8.0 Image  Graph Origin50.Graph0Origin GraphRoot EntrydO)0`UriZ@Pictures Current User5SummaryInformation(PT      !"#$%&'()*+,-./0123456789:;<=>?@AZ _gDraganaDraganae[imir Mol;anov    Custom   ArialTahoma WingdingsTimes New Roman TexturedCorel PHOTO-PAINT 8.0 Image Origin GraphCS ChemDraw DrawingSlide 1  Fonts U      !"#$%&'()*+,-./0123456789:;<=>?@ABCDEFGHIJKLMNOPQRSTUVWXw[]^_`abcdefghijklmnopqrstuvxyz{|}~BPb$I=eJ|{X2$Џtݫ14p2$aD$)}#Aev"fX$R$t'Q^'a,Y(R$b~ K0@w ;2$Ul֝%|_(UR2$y1e7[t?b$w'nfzR??VeVB| 2$*|Ag:+J5RvR$W3VN::U5@'uT2$|7z` փP$$$$b$8#2| CQ2$mj*:t} $+$2$p[tͰvM 6$2$+&oɵ2 {Ү?8QC C 0AA f@8:;wNO ʚ;`8ʚ;g4ddj 0"h p(5p'<4dddd w 0Tp,<4!d!d w 0Tp, 80___PPT10 ppX  |?; 0L0 >> -<  =(    <&KKA PIntramolecular photocyclization of new dithiophene-substituted o-divinylbenzenes>Q ?HHHh            <A i??"`!   i>  <?KHw 0D.Vidakovi 1), K. Mol anov 2), B. Koji-Prodi 2), M. `indler-Kulyk 1) 1)Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Maruliev trg 19, 10 000 Zagreb, Croatia 2)Laboratory for Chemical and Biological Crystallography, Department of Physical Chemistry, The Ruer Boakovi Institute, Bijeni ka cesta 54, 10 000 Zagreb,Croatia dragana.vidakovic@fkit.hr  ((((((((($$$$           i      `                 <(JKqL `Thiophenes and their polycyclic derivatives represent a class of important and well-studied heterocycles [1]. The interest in this kind of compounds has spread from early dye chemistry to modern drug design and self-assembled superstructures. Unsaturated thiophene derivatives show a versatile photoreactivity and formations of various photoproducts with remarkable electrochemical, optical, physical and biological properties [1]. $$$h  R        |   <XdK L 6In aim to investigate the effect of sulphur moiety on photobehaviour of dithiophene-substituted o-divinylbenzenes, the novel 2,2'-(1,2-phenylenedivinylene)dithiophene (3), 2,2'-(1,2-phenylenedivinylene)-5,5'-dimethyldithiophene (4) and 2,2'-(1,2-phenylenedivinylene)-5,5'-dibromodithiophene (5) were prepared, and compared with previously investigated difuro-substituted o-divinylbenzenes [2]. `$$G$$<$$>$$N$$$6        7 <  8          g   <|K'FL1 AContrary to these results, novel thiophene analogs 3-5 upon irradiation gave completely different photoproducts, the only observed products were dihydronaphtalenes (6-8), with traces of cyclophane (9). Formation of dihydronaphtalenes 6-8 could be explained by [1,6] electrocyclization and subsequent 1,5-H shift (scheme 2). According to this mechanism, replacement of the furan moiety with thiophene, which is more aromatic than furan, may have influence on the excited state properties of this new hexatriene system and as concequence the formation of diverse photoproducts .,E3$$$$o$$$$$$$$$$$$<$$$j                             ,      " G8 tkR '16Z  ZeeA  ??"`80?  K@ tkR >tkR@ O O  ZeeA  ??"`Y/    ZeeA ??"`@O L  HpKee"`"h #  cis,cis-3aP 0@ 4  HpKee"`b3 b4  cis,trans-3bP 0&  B  HtKee"`UCJ UD trans,trans-3cP02 i  6xKPtkR MFigure 1. Photoisomerization of 2,2'-(1,2-phenylenedivinylene)dithiophene (3)8N  DR +  6  <LK\u7` [1] E. Campaigne, Thiophenes and their Benzo Derivatives: (iii) Synthesis and Applications in A.R. Katritzky (ed) Comprehensive Heterocyclic Chemistry; vol. 4, Part 3, Pergamon Press, Oxford 1984., 863-934. [2] I. `kori, N. Basari, }. Marini, A. Vianjevac, B. Koji-Prodi and M. `indler, Chem. Eur. J. 2005, 11, 543-551.G r $   !  c       J         7   <                    s JA   f&logo1CECP 2006"`d[ f  0 ! 6TKbf6/g ?a"Central European Conference on Photochemistry" 10th-14th February, 2008 Bad Hofgastein, Austria<b 1$$$~0   ' s PA $ f&pic_badhofgastein"`b#CK$g  0I8 <NKCG[ NK<CG[j  S ,A plakat"`B1NKCXp  S 2A ORTEP002b"`j|K.X  6K <XBG[ Figure 2. Molecular structure of photoproduct 6 (left) as determined by X-ray crystallography. The molecules in crystals are disordered over two positions (right)..            0\v&% oIn the case of 2,2'-(1,2-phenylenedivinylene)difuran (1), during irradiation intramolecular [2+2] cycloaddition and intermolecular photocyloaddition took place to give bicyclo[3.2.1.]octadiene (2) and cyclobutane dimers as main products, respectively [2].X 6$$$$=$         8 2 3J 2 3J+ ( H@"`gH$J Sheme 2. Photoreactivity of 3-5, .   BA ??"`2 3.I ,8 D40M.J 03M.JH ) < D4GM.J vFigure 3. 1H NMR spectra (in CDCl3. 300 and 600 MHz) of the aliphatic region of three new dihydronaphtalenes (6, 7, 8)pw  U   T 3-JA # 40M2G`@ 3-J22 3-J22z 4 <A?"`3?.J22  <A s??"`X8-m:/ s`@ 3>JA 3>JAz 5 <A? "`3>JA  <A t??"`81>#;? t`@ 33J)= 33J)=z 6 <A ?"`33J)=  <A u??"`88^;L: u8 )G' )H'  <A ~??)G}% ~.  <)%]6' Scheme 1. Photoreactivity of 1<  <R  C *A IRB-logoCL v  PA [ ?h_009a"@` 3380___PPT10.Y`Zr&_(g1