Stable Alkali-Metal Complexes of Hybrid Disila-Crown Ethers

被引:31
|
作者
Reuter, Kirsten [1 ,2 ]
Buchner, Magnus R. [1 ,2 ]
Thiele, Guenther [3 ]
von Haenisch, Carsten [1 ,2 ]
机构
[1] Univ Marburg, Fachbereich Chem, Hans Meerwein Str 4, D-35032 Marburg, Germany
[2] Univ Marburg, WZMW, Hans Meerwein Str 4, D-35032 Marburg, Germany
[3] Univ Calif Berkeley, Dept Chem, 210 Lewis Hall, Berkeley, CA 94720 USA
关键词
RING-OPENING POLYMERIZATION; BASIS-SETS; DENSITY; SILOXANES; APPROXIMATION; BASICITY; ENERGY; BOND;
D O I
10.1021/acs.inorgchem.6b00267
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The complexation ability of hybrid disilane and ethylene containing crown ether ring systems was analyzed using 1,2-disila[12]crown-4 (1), 1,2-disila[15]crown-5 (2), 1,2-disila[18]crown-6 (3), and 1,2,7,8-tetrasila[12]crown-4 (7). Alkali-metal complexes (Li+, Na+, K+) were obtained and analyzed via X-ray diffraction. The complex stability of [Li(1,2-disila[12]crown-4)]+ and [Li(1,2,7,8-tetrasila[12]crown-4)]+ was determined, in relation to the lithium complex of [12]crown-4, by density functional theory (DFT) calculations employing the BP86/def2-TZVP level of theory. In solution, the exchange of lithium cations between pure [12]crown-4 and hybrid [12]crown-4 is on even terms, as has been shown from the relative binding affinity of compounds 1 and 7 by means of dynamic proton nuclear magnetic resonance (NMR) spectroscopy.
引用
收藏
页码:4441 / 4447
页数:7
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