1990
DOI: 10.1016/s0277-5387(00)84295-3
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Synthesis, characterization and structural aspects of diorganotellurium(IV) compounds containing (TeS) bonds

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Cited by 14 publications
(14 citation statements)
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“…The downfield chemical shift in comparison to that of free ligands (Table 1) indicates a considerable drift of electron density from the phosphorus to the tin atom through the oxygen atom. [14] Noticeable chemical shift differences are observed for PhP(O)(NH t Bu) 2 (Table 1) in varying the solvent. This difference is also related to the poor hydrogen bonding of CDCl 3 with electronegative atoms compared with DMSO-d 6 .…”
Section: Synthesis and Spectral Characterizationmentioning
confidence: 96%
“…The downfield chemical shift in comparison to that of free ligands (Table 1) indicates a considerable drift of electron density from the phosphorus to the tin atom through the oxygen atom. [14] Noticeable chemical shift differences are observed for PhP(O)(NH t Bu) 2 (Table 1) in varying the solvent. This difference is also related to the poor hydrogen bonding of CDCl 3 with electronegative atoms compared with DMSO-d 6 .…”
Section: Synthesis and Spectral Characterizationmentioning
confidence: 96%
“…Several reports on organotellurium (IV) compounds with 1,1-dithioligands are known, including O-alkyl-dithiocarbonate [1][2][3], N,N-dialkyl-dithiocarbamates [4][5][6][7], O,O-dialkyl and alkylene dithiophosphates [8][9][10][11][12][13][14][15]. They exhibit a great structural diversity due mainly to the strong inclination to form supramolecular associations through inter-and intramolecular Te-donor atom interactions and to the apparently stereochemically active lone pair at the tellurium center.…”
Section: Introductionmentioning
confidence: 99%
“…The downfield chemical shift in comparison to that of free acid indicates a considerable drift of electron density from the phosphorus to the tin atoms through the oxygen atoms [9].…”
Section: Nmrmentioning
confidence: 92%
“…{[Me 2 ClSnO 2 P(OC 2 H 5 ) 2 ] 2 } n 5 Sn(1)-C (9) 2.104 (16) Sn (2)-C(11) 2.073 (14) Sn (1)-C(10) 2.126 (15) Sn (2)-C(12) 2.055 (15) Sn (1)-Cl (1) 2.351 (7) Sn (2)-Cl (2) 2.399 (7) Sn (1)-O(1) 2.200 (9) Sn (2) (4) 1.546(6) P(2)-O(8) 1.541(7) C(9)-Sn(1)-C (10) 144.2(7) C(12)-Sn(2)-C(11) 152.1(7) C(9)-Sn(1)-Cl (1) 110.8(5) C(11)-Sn(2)-Cl(2) 101.3(5) C(10)-Sn(1)-Cl (1) 104.7(5) C(12)-Sn(2)-Cl(2) 106.6(5) O(1)-Sn (1) (14) C(13)-Sn(1)-C (9) 142.7(9) C(21)-Sn(2)-C(17) 143.8(8) C(9)-Sn(1)-Cl (1) 108.1(6) C(17)-Sn(2)-Cl (2) 108.2(6) C(13)-Sn(1)-Cl (1) 109.0(6) C(21)-Sn(2)-Cl(2) 107.8(6) O(6)#1-Sn (1) Symmetry code for complex 5: #1 x + 1/2, Ày + 3/2, z. Symmetry code for complex 8: #1 x + 1, y, z. Fig.…”
Section: 12mentioning
confidence: 99%