Solution and cross-polarization/magic angle spinning NMR investigation of intramolecular coordination Sn-N in some organotin(IV) C,N-chelates

被引:64
作者
Ruzicka, A
Jambor, R
Brus, J
Cisarová, I
Holecek, J
机构
[1] Univ Pardubice, Fac Chem Technol, Dept Gen & Inorgan Chem, CZ-53210 Pardubice, Czech Republic
[2] Acad Sci Czech Republ, Inst Macromol Chem, CR-16206 Prague 6, Czech Republic
[3] Charles Univ, Fac Nat Sci, Prague 12840 2, Czech Republic
关键词
C; N-chetates; NMR spectroscopy; intramolecular interaction; X-ray diffraction;
D O I
10.1016/S0020-1693(01)00596-5
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
An intramolecular donor/acceptor Sn-N bonding connection in a set of triphenyl- and diphenyl-(halogeno)tin(IV) C,N-chelates. Ph2XSnL, where Ph = C6H5, X = Ph, Cl or Br and L' = 2-(dimethylaminomethyl)phenyl-, C6H,(CH,NMe,)-2. and L' = 2,6-bis[(dimethylaminomethyl)phenyll-, C H ',(CH,NMe1)2-2,6, respectively, was studied by "'Sn, 'N, "C and 'H NMR spectroscopy in solution of non-coordinating solvent (CDCI,) and by "'Sn cross-polarization ' imagic angle spinning NMR techniques in the solid-state. The existence of Sn-N coordination bonds was confirmed in studied compounds and their strengths were evaluated through the values of NMR spectra parameters of nuclei directly involved in Sn-N connection, namely by characteristic changes of chemical shifts 6('"'Sn) and 5(`N) and values of J('"Sn. '3Q and J("'Sn, 'N) coupling constants. The set was extended by compound [2,6-C1H3(CH,NMe,),jPhSnCl, (5a), that is the decomposition product of compound [2,6-C,H3(CH,NMe,),]Ph,SnCl (5), This 5a was characterized by NMR spectroscopy and its structure was estimated by X-ray diffraction techniques. O 2001 Elsevier Science B.V. All rights reserved.An intramolecular donor/acceptor Sn-N bonding connection in a set of triphenyl- and diphenyl-(halogeno)tin(IV) C,N-chelates. Ph2XSnL, where Ph = C6H5, X = Ph, Cl or Br and L-1 = 2-(dimethylaminomethyl)phenyl-, C6H4(CH2NMe2)-2, and L-2 = 2,6-bis[(dimethylaminomethyl)phenyl]-, C6H3(CH2NMe2)(2)-2,6, respectively, was studied by Sn-119, N-15, C-13 and H-1 NMR spectroscopy in solution of non-coordinating solvent (CDCl3,) and by Sn-119 cross-polarization/magic angle spinning NMR techniques in the solid-state. The existence of Sn-N coordination bonds was confirmed in studied compounds and their strengths were evaluated through the values of NMR spectra parameters of nuclei directly involved in Sn-N connection, namely by characteristic changes of chemical shifts delta(Sn-119) and delta(N-15) and values of J(Sn-119, C-13 and J(Sn-119, C-13) coupling constants. The set was extended by compound [2,6-C6H3(CH2NMe2)(2)]PhSnCl2 (5a), that is the decomposition product of compound [2,6-C6H3(CH2NMe2)(2)]Ph2SnCl (5), This 5a was characterized by NMR spectroscopy and its structure was estimated by X-ray diffraction techniques. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:163 / 170
页数:8
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