Detailed Information on Publication Record
2004
Intramolecular Triplet-Triplet Energy Transfer in Short Flexible Bichromophoric Amino Acids, Dipeptides and Carboxylic Acid Diester
ZABADAL, Miroslav, Petr KLÁN, Dominik HEGER and Zdeněk KŘÍŽBasic information
Original name
Intramolecular Triplet-Triplet Energy Transfer in Short Flexible Bichromophoric Amino Acids, Dipeptides and Carboxylic Acid Diester
Name in Czech
Intramolekulární tripletový přenos energie u krátkých bichromoforních aminokyselin
Authors
ZABADAL, Miroslav (203 Czech Republic), Petr KLÁN (203 Czech Republic, guarantor), Dominik HEGER (203 Czech Republic) and Zdeněk KŘÍŽ (203 Czech Republic)
Edition
Collect. Czech. Chem. Commun. Praha, 2004, 0010-0765
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10401 Organic chemistry
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 1.062
RIV identification code
RIV/00216224:14310/04:00009947
Organization unit
Faculty of Science
UT WoS
000220854200004
Keywords in English
photochemistry; energy transfer
Tags
International impact
Změněno: 23/6/2009 15:42, prof. RNDr. Petr Klán, Ph.D.
V originále
Efficiencies of the intramolecular triplet-triplet energy transfer (ITET) in various bichromophoric amino acids (glycine, valine, phenylalanine, and sarcosine), dipeptides (glycylglycine, phenylalanylphenylalanine), and a simple diester, with the benzoyl and naphthyl terminal groups serving as donor and acceptor, respectively, have been determined by the steady-state photokinetic measurements. The magnitude of the transfer rate constants (>10 exp8 s-1) and the number of bonds separating the chromophores (8 or 11 atoms) suggest a through-space exothermic exchange mechanism in all cases. The influence of interchromophore distance, the character of the connecting chain as well as of side chains, was evaluated. While the most efficient energy transfer was found in a flexible diester and in valine- and sarcosine-based molecules due to the steric effect of the side hydrocarbon groups, the benzyl groups in the phenylalanine and phenylalanylphenylalanine-based bichromophores had a suppressing effect on ITET. Rigidity of the peptide bond in short bichromophoric compounds causes that a large number of favorable geometries preexist already before excitation; thus the intramolecular processes are controlled by ground-state conformational distribution. Replacing this bond by a less rigid ester moiety would allow that certain unfavorable conformations may coil to favorable ones within the excited-state lifetime (a rotation-controlled photochemical model). Some conclusions were supported by a conformational search of the potential energy surface and molecular dynamics simulations.
In Czech
Intramolekulární tripletový přenos energie u krátkých bichromoforních aminokyselin
Links
MSM 143100005, plan (intention) |
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