2004
DOI: 10.1016/j.jorganchem.2003.09.035
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Simplified synthesis, 1H, 13C, 15N, 119Sn NMR spectra and X-ray structures of diorganotin(IV) complexes containing the 4-phenyl-2,4-butanedionebenzoylhydrazone(2−) ligand

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Cited by 26 publications
(9 citation statements)
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References 28 publications
(59 reference statements)
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“…5 together with the atomic Table 2 Selected bond distances (Å ) and angles (°) for [H 2 L 2 ] (14) 107.60 (18) (14) 108.39(18) C(10)-C(9)-N(2) 119.8(4) N(2)-S(1)-C (14) 107.35(15) C(8)-C(9)-N(2) 119.8(3) C(7)-N(1)-C (8) 118.6(3) C(9)-N(2)-S(1) 120.8 (2) Hydrogen bonds for H 2 L 2 (Å and deg) (1) 0.90 (7) 1.89 (6) 2.649(4) 141(5) N(2)-H(2)Á Á ÁO(2) #1 0.83 (5) 2.32 (5) 3.030 (4) 143 (4) Symmetry transformations used to generate equivalent atoms: #1 Àx + 1, y, Àz. ( 104.90(11) N(2)-C(5)-C(4) 122.5(2) O(1)-S(1)-C (12) 107.85(10) C(5)-N(2)-C (6) 121.10(19) O(2)-S(1)-C (12) 108.26(11) C(11)-N(3)-S(1) 123.03 (16) Hydrogen bonds for [H 2 L 1 ] (Å and deg)…”
Section: Synthesismentioning
confidence: 99%
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“…5 together with the atomic Table 2 Selected bond distances (Å ) and angles (°) for [H 2 L 2 ] (14) 107.60 (18) (14) 108.39(18) C(10)-C(9)-N(2) 119.8(4) N(2)-S(1)-C (14) 107.35(15) C(8)-C(9)-N(2) 119.8(3) C(7)-N(1)-C (8) 118.6(3) C(9)-N(2)-S(1) 120.8 (2) Hydrogen bonds for H 2 L 2 (Å and deg) (1) 0.90 (7) 1.89 (6) 2.649(4) 141(5) N(2)-H(2)Á Á ÁO(2) #1 0.83 (5) 2.32 (5) 3.030 (4) 143 (4) Symmetry transformations used to generate equivalent atoms: #1 Àx + 1, y, Àz. ( 104.90(11) N(2)-C(5)-C(4) 122.5(2) O(1)-S(1)-C (12) 107.85(10) C(5)-N(2)-C (6) 121.10(19) O(2)-S(1)-C (12) 108.26(11) C(11)-N(3)-S(1) 123.03 (16) Hydrogen bonds for [H 2 L 1 ] (Å and deg)…”
Section: Synthesismentioning
confidence: 99%
“…The distortion is mainly due to the rigidity of the five-membered N(1)-Sn(1)-N(2) chelate rings, with angles of 73.15 (12)°and 73.43(9)°(average value) in 3 and 4, respectively.…”
Section: Molecular Structure Of [Snme 2 L 2 ] (3) and [Snph 2 L 2 ] (4)mentioning
confidence: 99%
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“…Recently these compounds have been used in new contexts as in cancer chemotherapy [22,23]. In view of a few reports on organotin(IV) complexes of hydrazones derived from 1,3-diketones [24][25][26][27][28], it was considered worthwhile to investigate the synthesis, structural aspects and biological properties of hydrazonic derivatives of 1,3-diketones and their organotin complexes. In the present paper, 2-furancarboxylic acid hydrazone derivative of benzoyl acetone and its dimethyl-and diphenyltin complexes have been synthesized.…”
Section: 3-diketones Constitute An Important Class Of Compounds Whmentioning
confidence: 99%
“…[11][12][13] In particular, complexes with Schiff bases derived from amino acids [14][15][16] and ONO and NNO tridentate dianionic Schiff bases have been widely reported. [17][18][19][20] This type of ligand typically acts as a multidentate planar chelating agent coordinating through the phenolic and amide oxygens and imine nitrogen.…”
Section: Introductionmentioning
confidence: 99%