Naslov
Conformational Analysis of beta-Lactam-Containing Ferrocene Peptides

Autori
Kovač, Veronika ; Radolović, Katarina ; Habuš, Ivan ; Siebler, Daniel ; Heinze, Katja ; Rapić, Vladimir

Izvornik
European journal of inorganic chemistry (1434-1948) 12 (2009), 3; 389-399

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
conformation analysis ; density functional calculations ; hydrogen bonds ; metallocenes ; molecular modeling

Sažetak
The homochiral 3-amino-1-(4-methoxyphenyl)-4-phenyl-beta-lactam (≡ Alm) was conjugated with Boc-Ala giving Ala-Alm (9) after Boc-deprotection (Boc = tert-butoxycarbonyl, Ala = alanine). Coupling of FcCOOH (1) and Boc-Fca (10) with “ dipeptide” 9 resulted in the formation of FcCO-Ala-Alm (12) and the trisamide Boc-Fca-Ala-Alm (13), respectively (Fc = ferrocenyl, Fca = 1’ -aminoferrocene-1-carboxylic acid). The reactions were accomplished by the HOBt/EDC procedure and the products were obtained in good yields (HOBt = 1-hydroxybenzotriazole, EDC = N-(3-dimethylaminopropyl)-N’ -ethylcarbodiimide hydrochloride). Symmetrically 1, 1’ -disubstituted “ tetrapeptide” Fn(CO-Ala-Alm)2 (14) was prepared by reaction of ferrocene chloride 11 with 9 (Fn = 1, 1’ -ferrocenediyl). Spectroscopic and theoretical analyses revealed that compounds 12, 13, and 14 are stabilized in solution by medium strong intramolecular hydrogen bonds. In all dominant conformations (DFT calculations) intrachain bonds spanning COFc and NHAlm are present (gama-turns). Additional interchain hydrogen bonds NHAla• • • COBoc (13) and NHAla• • • COAla / NHAla• • • COAlm (14) give rise to ordered helical conformations of the ferrocene moieties.

Izvorni jezik
Engleski

Znanstvena područja
Kemija

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