Pregled bibliografske jedinice broj: 347439
Theoretical study of hydrogen bonding in disubstituted ferrocene peptides using AIM theory and NBO analysis
Theoretical study of hydrogen bonding in disubstituted ferrocene peptides using AIM theory and NBO analysis // Book of abstracts, The 2nd Opatija Meeting on Computational Solutions in the Life Sciences / Babić Darko ; Došlić, Nađa ; Smith, David ; Tomić, Sanja ; Vlahoviček, Kristijan (ur.).
Zagreb: Institute of Computational Life Sciences (ICLS), 2007. (poster, nije recenziran, sažetak, znanstveni)
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Naslov
Theoretical study of hydrogen bonding in disubstituted ferrocene peptides using AIM theory and NBO analysis
Autori
Kodrin, Ivan ; Mihalić, Zlatko ; Rapić, Vladimir
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of abstracts, The 2nd Opatija Meeting on Computational Solutions in the Life Sciences
/ Babić Darko ; Došlić, Nađa ; Smith, David ; Tomić, Sanja ; Vlahoviček, Kristijan - Zagreb : Institute of Computational Life Sciences (ICLS), 2007
ISBN
978-953-6690-69-5
Skup
The 2nd Opatija Meeting on Computational Solutions in the Life Sciences
Mjesto i datum
Opatija, Hrvatska, 04.09.2007. - 09.09.2007
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
ferrocene peptides; hydrogen bonds; DFT
Sažetak
Ferrocene-containing derivatives of asymmetrically substituted 1, 1'-dicarboxylic acid with natural amino acids can create hydrogen-bonded structures that result in organised helical ferrocene units in solution. In this study we present the results of theoretical investigations of interactions within previously synthesized asymmetrical 1, 1'-disubstitu-ted ferrocene peptides of type I, MeCO-Fn-CO-AA-OMe, and type II conjugates, MeCO-Fn-CO-AA-NHMe (Fn = ferrocene-1, 1'-diyl, AA = L-α -amino acid, Gly, Ala or Val). A detailed population analysis of the several most stable conformers of each model type was performed with natural bond orbitals (NBO) and atoms in molecules (AIM) methods on previously optimized geometries with B3LYP/6-311G(d, p) and LanL2DZ basis set at Fe atom. Molecules were classified by the criteria of similarity of the inherent hydrogen bonds. Geometrical, topological and energetic properties of hydrogen bonds at the bond critical points (BCP) were compared. With few exceptions, observed proper N− H• • • O and improper C− H• • • O hydrogen bonds can be classified as weak bonds. Relative stability of equivalent conformers does not depend on specific amino acid and can be correlated with the number and type of hydrogen bonds.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
119-1191342-1339 - Molekulsko modeliranje strukture i reaktivnosti organskih spojeva (Mihalić, Zlatko, MZOS ) ( CroRIS)
058-1191344-3122 - Metalocenski biokonjugati, heterocikli i makromolekule (Kovač, Veronika, MZOS ) ( CroRIS)
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb