Synthesis, crystal structure and computational studies of new steroidal hemisuccinyl ester derivatives

被引:2
|
作者
Ramirez-Lozano, Claudia M. [1 ]
Eugenia Ochoa, Ma [1 ]
Labra-Vazquez, Pablo [2 ]
Farfan, Norberto [3 ]
Santillan, Rosa [1 ]
机构
[1] IPN, Ctr Invest & Estudios Avanzados, Dept Quim, Apdo Postal 14-740, Mexico City 07000, DF, Mexico
[2] CNRS, Lab Chim Coordinat LCC, 205 Route Narbonne,BP44099, F-31077 Toulouse 4, France
[3] Univ Nacl Autonoma Mexico, Fac Quim, Dept Quim Organ, Cdmx 04510, Mexico
关键词
Steroids; Hemiesters; Hydrogen bonding; Supramolecular; DFT; X-Ray structure; HYDROGEN-BONDS; GEOMETRY; CONFORMATION; INHIBITORS; MOLECULES; ACETATE; ACID; DHEA; SET;
D O I
10.1016/j.molstruc.2022.134191
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The synthesis and characterization of steroidal hemisuccinate esters derived from pregnanolone, pregnenolone, 3 beta,19-dihydroxy-androst-5-en-17-one and cholic acid are presented. A combined theoreticalexperimental analysis of the conformation and self-assembly of the crystalline samples is carried out with support from single crystal X-ray diffraction experiments and DFT computations, featuring CremerPople ring puckering and Quantum Theory of Atoms-in-Molecules (QTAIM) analyses, unveiling a proclivity of these molecules towards the formation of dimeric and trimeric supramolecular assemblies bound by means of classical and non-classical hydrogen bonding interactions, whose directionality and energetics are discussed in detail within reduced systems of the crystallographic structures. (c) 2022 Elsevier B.V. All rights reserved.
引用
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页数:15
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