TY  - JOUR
AU  - Miodragović Đenana U.
AU  - Milosavljević, Slobodan M.
AU  - Malinar, M.J.
AU  - Celap, MB
AU  - Todorović, Nevena M.
AU  - Juranić, N.
PY  - 2002
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/537
AB  - Rotamer population of S-tyrosinato and S-phenylalaninato ligands side groups in diastereomers of (1,2-diaminoethane)bis(S-aminocarboxylato)cobalt(III) complexes is calculated by vicinal alpha and beta proton coupling constant analysis. The effect of noncovalent intra- and interligand interactions on the population of rotamers in D2O solution is discussed. It has been established that in all the complexes investigated the most abundant is rotamer t, in which aromatic voluminous moiety and carboxylic group are in an anti position. In almost all complexes the lowest content is of rotamer g, in which these two groups are in the nearest position. Relatively high population of rotamer b in complex 5 tyr, in spite of high steric hindrances, is due to intra- and interligand NH... pi interactions.
PB  - Taylor & Francis Ltd, Abingdon
T2  - Enantiomer
T1  - Mixed cobalt(III) complexes with aromatic amino acids and diamine. Part IV. Influence of noncovalent intraand interligand interactions on rotamer population of the S-phenylalaninato and S-tyrosinato side groups in (1,2-diaminoethane)bis(S-aminocarboxylato
VL  - 7
IS  - 6
SP  - 375
EP  - 382
DO  - 10.1080/10242430215714
ER  - 

@article{
author = "Miodragović Đenana U. and Milosavljević, Slobodan M. and Malinar, M.J. and Celap, MB and Todorović, Nevena M. and Juranić, N.",
year = "2002",
abstract = "Rotamer population of S-tyrosinato and S-phenylalaninato ligands side groups in diastereomers of (1,2-diaminoethane)bis(S-aminocarboxylato)cobalt(III) complexes is calculated by vicinal alpha and beta proton coupling constant analysis. The effect of noncovalent intra- and interligand interactions on the population of rotamers in D2O solution is discussed. It has been established that in all the complexes investigated the most abundant is rotamer t, in which aromatic voluminous moiety and carboxylic group are in an anti position. In almost all complexes the lowest content is of rotamer g, in which these two groups are in the nearest position. Relatively high population of rotamer b in complex 5 tyr, in spite of high steric hindrances, is due to intra- and interligand NH... pi interactions.",
publisher = "Taylor & Francis Ltd, Abingdon",
journal = "Enantiomer",
title = "Mixed cobalt(III) complexes with aromatic amino acids and diamine. Part IV. Influence of noncovalent intraand interligand interactions on rotamer population of the S-phenylalaninato and S-tyrosinato side groups in (1,2-diaminoethane)bis(S-aminocarboxylato",
volume = "7",
number = "6",
pages = "375-382",
doi = "10.1080/10242430215714"
}

Miodragović Đenana U., Milosavljević, S. M., Malinar, M.J., Celap, M., Todorović, N. M.,& Juranić, N.. (2002). Mixed cobalt(III) complexes with aromatic amino acids and diamine. Part IV. Influence of noncovalent intraand interligand interactions on rotamer population of the S-phenylalaninato and S-tyrosinato side groups in (1,2-diaminoethane)bis(S-aminocarboxylato. in Enantiomer
Taylor & Francis Ltd, Abingdon., 7(6), 375-382.
https://doi.org/10.1080/10242430215714

Miodragović Đenana U., Milosavljević SM, Malinar M, Celap M, Todorović NM, Juranić N. Mixed cobalt(III) complexes with aromatic amino acids and diamine. Part IV. Influence of noncovalent intraand interligand interactions on rotamer population of the S-phenylalaninato and S-tyrosinato side groups in (1,2-diaminoethane)bis(S-aminocarboxylato. in Enantiomer. 2002;7(6):375-382.
doi:10.1080/10242430215714 .

Miodragović Đenana U., Milosavljević, Slobodan M., Malinar, M.J., Celap, MB, Todorović, Nevena M., Juranić, N., "Mixed cobalt(III) complexes with aromatic amino acids and diamine. Part IV. Influence of noncovalent intraand interligand interactions on rotamer population of the S-phenylalaninato and S-tyrosinato side groups in (1,2-diaminoethane)bis(S-aminocarboxylato" in Enantiomer, 7, no. 6 (2002):375-382,
https://doi.org/10.1080/10242430215714 . .