Unknown

Dataset Information

0

Electron transfer in Me-blocked heterodimeric alpha,gamma-peptide nanotubular donor-acceptor hybrids.


ABSTRACT: Bio-inspired cyclopeptidic heterodimers built on beta-sheet-like hydrogen-bonding networks and bearing photoactive and electroactive chromophores on the outer surface have been prepared. Different cross-strand pairwise relationships between the side chains of the cyclic alpha,gamma-peptides afford the heterodimers as three nonequivalent dimeric species. Steady-state and time-resolved spectroscopies clearly show an electron transfer process from pi-extended tetrathiafulvalene, covalently attached to one of the cyclopeptides, to photoexcited [60]fullerene, located on the complementary cyclopeptide. The charge-separated state was stabilized for up to 1 micros before recombining and repopulating the ground state. Our current example shows that cyclopeptidic templates can be successfully used to form light-harvesting/light-converting hybrid ensembles with a distinctive organization of donor and acceptor units able to act as efficient artificial photosystems.

SUBMITTER: Brea RJ 

PROVIDER: S-EPMC1838467 | biostudies-literature | 2007 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Electron transfer in Me-blocked heterodimeric alpha,gamma-peptide nanotubular donor-acceptor hybrids.

Brea Roberto J RJ   Castedo Luis L   Granja Juan R JR   Herranz M Angeles MA   Sánchez Luis L   Martín Nazario N   Seitz Wolfgang W   Guldi Dirk M DM  

Proceedings of the National Academy of Sciences of the United States of America 20070319 13


Bio-inspired cyclopeptidic heterodimers built on beta-sheet-like hydrogen-bonding networks and bearing photoactive and electroactive chromophores on the outer surface have been prepared. Different cross-strand pairwise relationships between the side chains of the cyclic alpha,gamma-peptides afford the heterodimers as three nonequivalent dimeric species. Steady-state and time-resolved spectroscopies clearly show an electron transfer process from pi-extended tetrathiafulvalene, covalently attached  ...[more]

Similar Datasets

| S-EPMC5512142 | biostudies-literature
| S-EPMC5510015 | biostudies-literature
| S-EPMC5333094 | biostudies-literature
| S-EPMC6844126 | biostudies-literature
| S-EPMC9189676 | biostudies-literature
| S-EPMC6006863 | biostudies-literature
| S-EPMC3210553 | biostudies-literature
2008-12-09 | GSE9830 | GEO
| S-EPMC8579843 | biostudies-literature
| S-EPMC521947 | biostudies-literature