2000
DOI: 10.1016/s0277-5387(00)00483-6
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Ligand reactivity, substituent effects and solvent interactions in the spectra and structure of some oxovanadium(V) chelates with Schiff bases. Proof for dimeric species

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Cited by 26 publications
(13 citation statements)
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“…Similar reactions of [VO(salpnol)Cl] (6) or [VO(ohacpnol)Cl] (7) with p-Me 3 SiC 6 H 4 SiMe 3 or p-Me 3 SiCH 2 C 6 H 4 CH 2 SiMe 3 yielded organo derivatives of oxovanadium(V) bridged by -C 6 H 4 -or -CH 2 C 6 H 4 CH 2 -(Scheme 1).…”
Section: Synthesesmentioning
confidence: 99%
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“…Similar reactions of [VO(salpnol)Cl] (6) or [VO(ohacpnol)Cl] (7) with p-Me 3 SiC 6 H 4 SiMe 3 or p-Me 3 SiCH 2 C 6 H 4 CH 2 SiMe 3 yielded organo derivatives of oxovanadium(V) bridged by -C 6 H 4 -or -CH 2 C 6 H 4 CH 2 -(Scheme 1).…”
Section: Synthesesmentioning
confidence: 99%
“…These lower (C¼N) values suggest stronger V-N bonding in the complexes. Despite complications due to the appearance of several bands in the infrared spectra of the ligands in the region 500-300 cm À1 , the presence of (V-Cl) in (2), (4), (6) and (8) can be identified around 360 cm À1 by careful comparison of the IR spectra of the free ligand and metal complexes. On the other hand, complexes 13-16 exhibit a peak at 320 cm À1 , which may be assigned to (V-Cl) stretching.…”
Section: Infrared Spectramentioning
confidence: 99%
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“…The complexes 2 and 3 display bands at 1468 and 687; 1462 and 681 cm -1 indicate the coordination of bipyridine and phenanthroline. In addition, the compounds exhibit a strong band in the 956-993 cm -1 region due to the terminal V=O stretching [19][20][21]. The electronic spectra of the complexes in DMF solution are presented in the Table 5.…”
Section: Crystal Structuresmentioning
confidence: 99%