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New acridinium trifluoromethanesulfonate stacks induced in the presence of organotin(IV) complexes

机译:在有机锡(IV)配合物的存在下诱导新的三氟甲烷磺酸methane啶叠层

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摘要

Three new crystalline architectures based on acridinium trifluoromethanesulfonate salts [C_(13)H_(10)N]~+[CF3SO3]~- have been isolated as single crystals from the reaction of the dimeric hydroxo di-n-butylstannane trifluoromethanesulfonato complex [n-Bu2Sn(OH) (H2O)(CF3SO3)]2 (1) with acridine (C_(13)H9N, Acr), in dichloromethane at room temperature. When an equimolar mixture of anthracene (C_(14)H_(10), Ant) and acridine is initially used, the crystallization of a sandwich-type arrangement occurs, leading to the intercalation of one molecule of anthracene between two acridium trifluoromethanesulfonate salt molecules. In the three X-ray structures reported, the crystal packing involves the contribution of hydrogen bonding and aromatic ring interactions, as well as short contacts of type O ···(H)C, F···(H)C and F···F.
机译:从二聚羟基二正丁基锡三氟甲烷磺酸盐络合物的反应中分离出了基于三氟甲烷磺酸a啶鎓盐[C_(13)H_(10)N] ++ [CF3SO3]-的三种新的晶体结构。在室温下于二氯甲烷中将Bu 2 Sn(OH)(H 2 O)(CF 3 SO 3)] 2(1)与a啶(C_(13)H 9 N,Acr)一起使用。最初使用蒽(C_(14)H_(10),Ant)和a啶的等摩尔混合物时,会发生夹心型排列的结晶,导致蒽分子的一个分子插入两个三氟甲基磺酸cri啶鎓盐分子之间。在报道的三个X射线结构中,晶体堆积涉及氢键和芳环相互作用的贡献,以及O···(H)C,F···(H)C和F·型的短接触··F。

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