首页> 外文期刊>Acta crystallographica. Section F, Structural biology communications >Three tetracyclic dibenzoazepine derivatives exhibiting different molecular conformations, different patterns of intermolecular hydrogen bonding and different modes of supramolecular aggregation
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Three tetracyclic dibenzoazepine derivatives exhibiting different molecular conformations, different patterns of intermolecular hydrogen bonding and different modes of supramolecular aggregation

机译:三个四环二苯脲卓卓衍生物,其具有不同的分子构象,分子间氢键的不同模式和超分子聚集的不同模式

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The biological potential of compounds of the tricyclic dibenzo[b,e]azepine system has resulted in considerable synthetic efforts to develop efficient methods for the synthesis of new derivatives of this kind. (9RS,15RS)-9-Ethyl-11-methyl-9,13b-dihydrodibenzo[c,f]thiazolo[3,2-a]azepin-3(2H)-one, C19H19N-OS, (I), crystallizes as a kryptoracemate with Z' = 2 in the space group P2(1), with one molecule each of the (9R, 15R) and (9S,15S) configurations in the asymmetric unit, while (9RS, 15RS)-9-ethyl-7,12-dimethyl-9,13b-dihydrodibenzo[c,f]thiazolo[3,2-a]azepin-3(2H)-one, C20H21NOS, (II), crystallizes with Z' = 1 in the space group C2/c. Ethyl (13RS)-2-chloro-13-ethyl-4-oxo-8,13-dihydro-4H-benzo[5,6]azepino[3,2,1-ij]quinoline-5-carboxylate, C22H20ClNO3, (III), exhibits enantiomeric disorder in the space group P (1) over bar such that the reference site is occupied by the 13R and 13S enantiomers, with occupancies of 0.900 (6) and 0.100 (6). In each of the two independent molecules in (I), the five-membered ring adopts an envelope conformation, but the corresponding ring in (II) adopts a half-chair conformation, while the six-membered ring in the major form of (III) adopts a twist-boat conformation. The conformation of the seven-membered ring in each of (I), (II) and the major form of (III) approximates to the twist-boat form. The molecules of compound (I) are linked by two C-H center dot center dot center dot O hydrogen bonds to form two independent antiparallel C(5) chains, with each type containing only one enantiomer. These chains are linked into sheets by two C-H center dot center dot center dot pi(arene) hydrogen bonds, in which the two donors are both provided by the (9R, 15R) enantiomer and the two acceptor arene rings form part of a molecule of (9S, 15S) configuration, precluding any additional crystallographic symmetry. The molecules of compound (II) are linked by inversion-related C-H center dot center dot center dot pi(arene) hydrogen bonds to form isolated cyc
机译:三环二苯苯甲苯的化合物的生物潜力[B,E]偶氮体系导致了相当大的合成努力,为合成这种新衍生物的有效方法。 (9rs,15rs)-9-乙基-11-甲基-9,13b-dihydridibenzo [c,f]噻唑[3,2-a]偶氮戊戊四-3(2h) - 酮,C19H19N-OS,(I),结晶作为空间组P2(1)中的Z'= 2的氪气肿,在不对称单元中(9R,15R)和(9S,15S)配置中的每一个,而(9RS,15RS)-9-乙基-7,12-二甲基-9,13b-Dihydridibenzo [C,F]噻唑唑[3,2-A]偶氮-3(2H) - 酮,C20H21NO,(II),在空间组中用Z'= 1结晶C2 / c。乙基(13RS)-2-氯-13-乙基-4-氧代-8,13-二氢-4H-苯并[5,6]紫红素[3,2,1-IJ]喹啉-5-羧酸盐,C22H20ClNO3,( III),在空间组P(1)上在棒中表现出对映体疾病,使得参考部位由13R和13S对映体占据,其占占0.900(6)和0.100(6)的占用。在(i)中的两个独立分子中的每一个中,五元环采用包络构象,但(ii)中的相应环采用半椅兼容,而六元环以主要形式(III) )采用扭船构象。在(I),(II)中的每一个和(III)的主要形式中的七元环的构象近似于扭船形式。化合物(I)的分子由两个C-H中心点中心点中心点O氢键连接,形成两个独立的反平行C(5)链,每种类型仅含有一种对映体。这些链与两个CH中心点中心点中心点PI(芳烃)氢键相连,其中两种供体均由(9R,15R)对映体提供,并且两个受体芳烃环形成一部分分子(9S,15S)配置,排除任何额外的晶体对称性。化合物(II)的分子通过倒置相关的C-H中心点中心点中心点PI(芳烃)氢键连接,形成分离的Cyc

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