journal article·2006-01-19

Photochromic Switches Incorporated in Bridging Ligands: A New Tool to Modulate Energy‐Transfer Processes

P. Belser, L. De Cola, F. Hartl, V. Adamo, B. Bozic, Y. Chriqui, V. M. Iyer, R. T. F. Jukes, J. Kühni, M. Querol, S. Roma, N. Salluce

Advanced Functional Materials· Volume 16· Issue 2
Publisher page

Abstract

Abstract The thoughful construction of molecular switches has led to a gamut of supramolecular systems that can be used in molecular electronics. These include molecules based on thienylethenes, spiropyrans, fulgides, dithienylphenanthrolines, and diazafluorenes. This article reviews the recent developments made in the synthesis and characterization of all these systems, thereby allowing a comparative study to validate the viability of these switchable molecules on a nanoscale. Also, the drawbacks of each class are demonstrated and, at the same time, the remedies for further improvisation are prescribed. We have made an honest attempt to present an exhaustive account of all the different photochromic switches developed by us hitherto.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Photochromic and Fluorescence Chemistry · Photoreceptor and optogenetics research · Porphyrin and Phthalocyanine Chemistry

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (97)

Show source-provided references
1. Chem. Rev. · 2000 · 1683
2. 10.1002/1521-3773(20001002)39:19<3348::AID-ANIE3348>3.0.CO;2-X10.1002/1521-3773(20001002)39:19<3348::AID-ANIE3348>3.0.CO;2-X ↗
3. 10.1002/(SICI)1521-3773(19991018)38:20<3086::AID-ANIE3086>3.0.CO;2-D10.1002/(SICI)1521-3773(19991018)38:20<3086::AID-ANIE3086>3.0.CO;2-D ↗
4. K. E. Dexler Nanosystems. Molecular Machinery Manufacturing and Computation Wiley New York1992.
5. J.‐M. Lehn Supramolecular Chemistry: Concepts and Perspectives VCH Weinheim Germany1995.10.1002/3527607439 ↗
6. Comprehensive Supramolecular Chemistry(Ed: D. N. Reinhoudt) Pergamon New York1996.
7. Supramolecular Chemistry(Eds: V. Balzani L. De Cola) Kluwer Dordrecht The Netherlands1992.
8. 10.1016/S0010-8545(98)00198-210.1016/S0010-8545(98)00198-2 ↗
9. Rouvray D. · Chem. Ber. · 1998 · 34 · 26
10. Frontiers in Supramolecular Organic Chemistry and Photochemistry(Eds: H.‐J. Schneider H. Dürr) VCH Weinheim Germany1990.
11. F. Vögtle Supramolecular Chemistry Wiley New York1991.
12. V. Balzani F. Scandola Supramolecular Photochemistry Horwood Chichester UK1991.
13. P. J. Martin Introduction to Molecular Electronics Arnold Edwards London1995.
14. Molecular Electronic Devices(Eds: F. L. Carter R. E. Siatkowski H. Wohltjen) North‐Holland Amsterdam The Netherlands1988.
15. Special Issue on Molecular Materials in Electronic and Optoelectronic Devices Acc. Chem. Res.1999 32.10.1021/ar990033n ↗
16. Special Issue on Molecular Machines Acc. Chem. Res.2001 34.10.1021/ar010084w ↗
17. 10.1021/ja990044b10.1021/ja990044b ↗
18. 10.1021/jp962366x10.1021/jp962366x ↗
19. 10.1016/S0010-8545(98)00198-210.1016/S0010-8545(98)00198-2 ↗
20. 10.1016/S0010-8545(00)00331-310.1016/S0010-8545(00)00331-3 ↗
21. J. C. Crano R. J.Guglielmetti Organic Photochromic and Thermochromic Compounds Kluwer Dordrecht The Netherlands1999 Vols. 1 2.
22. B. L. Feringa Molecular Switches Wiley‐VCH Weinheim Germany2001.10.1002/3527600329 ↗
23. Photochromism: Molecules and Systems(Eds: H. Dürr E. Bouas‐Laurent) Elsevier Amsterdam The Netherlands1990.
24. 10.1021/jo00239a02210.1021/jo00239a022 ↗
25. 10.1021/cr980069d10.1021/cr980069d ↗
26. 10.1016/S0040-4020(97)00558-910.1016/S0040-4020(97)00558-9 ↗
27. 10.1002/chem.1995001050410.1002/chem.19950010504 ↗
28. 10.1021/jo00130a03510.1021/jo00130a035 ↗
29. 10.1021/jo010267w10.1021/jo010267w ↗
30. 10.1038/420759a10.1038/420759a ↗
31. 10.1021/ic035020r10.1021/ic035020r ↗
32. 10.1039/C3994000101110.1039/C39940001011 ↗
33. 10.1002/chem.1995001050510.1002/chem.19950010505 ↗
34. 10.1002/chem.1996002111210.1002/chem.19960021112 ↗
35. 10.1002/(SICI)1521-3765(19991105)5:11<3285::AID-CHEM3285>3.0.CO;2-Q10.1002/(SICI)1521-3765(19991105)5:11<3285::AID-CHEM3285>3.0.CO;2-Q ↗
36. 10.1002/1099-0682(200007)2000:7<1581::AID-EJIC1581>3.0.CO;2-210.1002/1099-0682(200007)2000:7<1581::AID-EJIC1581>3.0.CO;2-2 ↗
37. 10.1039/b101377g10.1039/b101377g ↗
38. 10.1002/1099-0712(200011/12)10:6<245::AID-AMO422>3.0.CO;2-O10.1002/1099-0712(200011/12)10:6<245::AID-AMO422>3.0.CO;2-O ↗
39. 10.1002/1521-4095(200103)13:5<347::AID-ADMA347>3.0.CO;2-910.1002/1521-4095(200103)13:5<347::AID-ADMA347>3.0.CO;2-9 ↗
40. 10.1002/1521-3773(20010504)40:9<1752::AID-ANIE17520>3.0.CO;2-W10.1002/1521-3773(20010504)40:9<1752::AID-ANIE17520>3.0.CO;2-W ↗
41. 10.1002/adma.20030491710.1002/adma.200304917 ↗
42. 10.1021/ja954266v10.1021/ja954266v ↗
43. 10.1021/ic020525n10.1021/ic020525n ↗
44. 10.1021/ja993873610.1021/ja9938736 ↗
45. 10.1002/cber.1992125113310.1002/cber.19921251133 ↗
46. 10.2533/00094290377767956910.2533/000942903777679569 ↗
47. 10.1016/j.ccr.2004.12.01510.1016/j.ccr.2004.12.015 ↗
48. 10.1021/ic035334e10.1021/ic035334e ↗
49. 10.1016/S0022-2313(99)00382-810.1016/S0022-2313(99)00382-8 ↗
50. 10.1016/0010-8545(88)80032-810.1016/0010-8545(88)80032-8 ↗
51. 10.1039/P2984000129310.1039/P29840001293 ↗
52. 10.1039/P2984000130310.1039/P29840001303 ↗
53. 10.1002/1521-4095(200103)13:5<347::AID-ADMA347>3.0.CO;2-910.1002/1521-4095(200103)13:5<347::AID-ADMA347>3.0.CO;2-9 ↗
54. 10.1002/1616-3028(200203)12:3<167::AID-ADFM167>3.0.CO;2-M10.1002/1616-3028(200203)12:3<167::AID-ADFM167>3.0.CO;2-M ↗
55. 10.1021/ja036306y10.1021/ja036306y ↗
56. 10.1039/b417026a10.1039/b417026a ↗
57. 10.1021/ja010058t10.1021/ja010058t ↗
58. 10.1021/ja005699n10.1021/ja005699n ↗
59. 10.1002/1521-4095(20020318)14:6<401::AID-ADMA401>3.0.CO;2-F10.1002/1521-4095(20020318)14:6<401::AID-ADMA401>3.0.CO;2-F ↗
60. 10.1021/ja982598510.1021/ja9825985 ↗
61. 10.1016/j.tetlet.2003.09.07810.1016/j.tetlet.2003.09.078 ↗
62. 10.1016/1010-6030(95)04113-X10.1016/1010-6030(95)04113-X ↗
63. 10.1021/cr980071510.1021/cr9800715 ↗
64. 10.1016/S0277-5387(02)01397-910.1016/S0277-5387(02)01397-9 ↗
65. 10.1021/cr980070c10.1021/cr980070c ↗
66. M. G. Heller inCRC Handbook of Organic Photochemistry and Photobiology(Eds: W. M. Horspool P.‐S. Song) CRC Press Boca Raton FL1995 p. 173.
67. Heller H. G. · Adv. Color Sci. Technol. · 2001 · 4 · 6
68. Yam V. W.‐W. · Organometallics · 2000 · 19 · 182
69. 10.1002/chem.20030548510.1002/chem.200305485 ↗
70. 10.1016/0009-2614(93)85139-F10.1016/0009-2614(93)85139-F ↗
71. 10.1039/p1985000095710.1039/p19850000957 ↗
72. 10.1002/1099-0682(200104)2001:4<1019::AID-EJIC1019>3.0.CO;2-610.1002/1099-0682(200104)2001:4<1019::AID-EJIC1019>3.0.CO;2-6 ↗
73. 10.1021/ic020420k10.1021/ic020420k ↗
74. 10.1021/ja047446q10.1021/ja047446q ↗
75. Mlochowski J. · Roczniki Chemii Ann. Soc. Chem. Polonorum · 1974 · 2145
76. 10.1016/S0040-4039(97)10223-410.1016/S0040-4039(97)10223-4 ↗
77. 10.1246/bcsj.63.131110.1246/bcsj.63.1311 ↗
78. 10.1021/jo00130a03510.1021/jo00130a035 ↗
79. R. B. Woodward R. Hoffmann The Conservation of Orbital Symmetry VCH Weinheim Germany1970.10.1016/B978-1-4832-3290-4.50006-4 ↗
80. 10.1021/jo00261a03510.1021/jo00261a035 ↗
81. 10.1023/A:101754080114410.1023/A:1017540801144 ↗
82. 10.1021/cr990022810.1021/cr9900228 ↗
83. 10.1021/ja993297d10.1021/ja993297d ↗
84. 10.1126/science.273.5282.168610.1126/science.273.5282.1686 ↗
85. 10.1021/ar000172110.1021/ar0001721 ↗
86. 10.1002/(SICI)1521-3773(19991203)38:23<3418::AID-ANIE3418>3.0.CO;2-V10.1002/(SICI)1521-3773(19991203)38:23<3418::AID-ANIE3418>3.0.CO;2-V ↗
87. 10.1016/S0040-4039(00)78887-310.1016/S0040-4039(00)78887-3 ↗
88. 10.1021/ic00020a00510.1021/ic00020a005 ↗
89. 10.1016/S0040-4039(00)79123-410.1016/S0040-4039(00)79123-4 ↗
90. 10.1021/ja00065a02310.1021/ja00065a023 ↗
91. 10.1055/s-1996-418310.1055/s-1996-4183 ↗
92. 10.1080/0039791960800376510.1080/00397919608003765 ↗
93. 10.1002/recl.1995114111910.1002/recl.19951141119 ↗
94. De Cola L. · Chimia · 1996 · 50 · 21410.2533/chimia.1996.214 ↗
95. 10.1002/recl.1993112061210.1002/recl.19931120612 ↗
96. 10.1021/ol017130c10.1021/ol017130c ↗
97. 10.1016/S0010-8545(02)00089-910.1016/S0010-8545(02)00089-9 ↗