The process of intramolecular charge separation was studied in three nearly identical donor-bridge-acceptor compounds (1-3) under jet-cooled conditions. Each consists of a vinylcyanonaphthalene group as a powerful electron acceptor and an anilino derivative as an electron donor, separated by a rigid
Conformational Dynamics of Charge-Transfer States in Donor−Bridge−Acceptor Systems
✍ Scribed by Xavier Y. Lauteslager; Ivo H. M. van Stokkum; H. John van Ramesdonk; Dick Bebelaar; Jan Fraanje; Kees Goubitz; Henk Schenk; Albert M. Brouwer; Jan W. Verhoeven
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 532 KB
- Volume
- 2001
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
Donor-acceptor compounds containing a phenylenediamine electron donor and a naphthalene, a cyanobenzene, or a cyanonaphthalene acceptor were studied. The two chromophores are connected by three different bridging units, consisting of CH 2 groups linked to a semiflexible piperidine or piperazine ring or to a rigid 2,5-diazabicyclo[2.2.1]heptane group. All donor-acceptor compounds show photoinduced charge separation, resulting in the formation of a compact charge-transfer (CCT) state in nonpolar solvents. The conformational change needed to arrive at this species is imposs- [a]
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## Abstract Charge transfer complexes are interfacial charge pairs residing at the donor–acceptor heterointerface in organic solar cell. Experimental evidence shows that it is crucial for the photovoltaic performance, as both photocurrent and open circuit voltage directly depend on it. For charge p