期刊
INORGANIC CHEMISTRY
卷 58, 期 16, 页码 10955-10964出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.9b01387
关键词
-
资金
- CSIR, India [01(2651)/12/EMR-II]
- UGC, India
- IIT Delhi
- DST(SERB), India
- DST-India
The study presents a rational synthesis of new dimethyltin carboxylates, Me2Sn(H(2)btec) (1), Me2Sn(btec)(0.5)(2), [Me2Sn(H2O)(2)(btec)(0.5)]center dot H2O (3), and [{Me2SnOSn(OH)Me-2}(Me2SnOH)(btec)(0.5)]center dot H2O (4), derived from tetratopic 1,2,4,5-benzenetetracarboxylic acid (H(4)btec). The method relies upon hydrothermal reaction (130 degrees C, 72 h) of dimethyltin dichloride and H(4)btec under optimized pH (2 < pH < 8) conditions that allow control over dimethyltin speciation in aqueous medium as well as degree of deprotonation of the tetrafuntional carboxylic acid. The formation of a three-dimensional assembly in 1 is assisted by the bridging bidentate (mu(2)) mode of the carboxylate and O-H center dot center dot center dot O hydrogen bonds involving -COOH groups. The structure represents a unique example of the diorganotin framework derived from a partially deprotonated polyfuntional carboxylic acid. The structure of 2 adopts a three-dimensional motif wherein each pair of mu(2)-carboxylate groups (designated by C1 and C4) of the tetraanionic ligand form different spatial arrangements. For 3, the formation of one-dimensional motif with eight-coordinated tin atoms is assisted by the anisobidentate character of the carboxylate groups. The structure of 4 includes linear chains comprised of [Me2Sn(mu(2)-OH)](2) and the carboxylate ligand which extend to a layered motif with symmetrically substituted ladder-like distannoxanes acting as linkers. The underlying nets of 1, 2, and 4 exhibit sqc11, scu(sqc170), and sql topologies, respectively. Notably, these assemblies are extremely robust and show no sign of degradation upon exposure to neutral as well as weakly acidic/basic aqueous medium for 7 days.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据