Dinake Pogisego, Prokhorova Polina E, Talanov Vladimir S, Butcher Ray J, Talanova Galina G
Department of Chemistry, Howard University, 525 College Street, NW, Washington, DC 2059, USA.
Acta Crystallogr Sect E Struct Rep Online. 2012 Apr 1;68(Pt 4):m460-1. doi: 10.1107/S1600536812010768. Epub 2012 Mar 21.
The structure of the title complex, [Na(2)(C(80)H(98)N(4)O(10)S(2))(H(2)O)]·4CH(3)CN, obtained after crystallization from aceto-nitrile, contains two formula units in the asymmetric unit (Z' = 2) and an estimated four mol-ecules of acetonitrile per calixarene moiety. It is unusual for two Na(+) ions to occupy the lower rims of the cone calix[4]arene, as in this case, with one Na(+) ion forming two O→ Na(+) coordinate bonds with the two but-oxy groups and four such bonds with the two N-dansyl carboxamide groups, forming six dative bonds between Na(+) and O. On the other hand, the other Na(+) ion forms only five O→Na(+) coordinate bonds on the far end of the calix[4]arene lower rim, bringing the two dansyl groups in close proximity with each other. There also appears to be an O→Na(+) coordination coming from a dangling water mol-ecule. The structure contained both resolved and poorly resolved solvent mol-ecules. The latter were treated using the SQUEEZE routine in PLATON [Spek (2009 ▶). Acta Cryst. D65, 148-155].
从乙腈中结晶后得到的标题配合物[Na₂(C₈₀H₉₈N₄O₁₀S₂)(H₂O)]·4CH₃CN的结构,其不对称单元中含有两个化学式单元(Z' = 2),每个杯芳烃部分估计有四个乙腈分子。在这种情况下,两个Na⁺离子占据杯[4]芳烃锥底的较低边缘是不寻常的,其中一个Na⁺离子与两个丁氧基形成两个O→Na⁺配位键,与两个N - 丹磺酰羧酰胺基团形成四个这样的键,在Na⁺和O之间形成六个配位键。另一方面,另一个Na⁺离子在杯[4]芳烃较低边缘的远端仅形成五个O→Na⁺配位键,使两个丹磺酰基团彼此靠近。似乎还有一个来自游离水分子的O→Na⁺配位。该结构包含解析度好和解析度差的溶剂分子。后者使用PLATON中的SQUEEZE程序进行处理[Spek (2009 ▶). Acta Cryst. D65, 148 - 155]。