2005
DOI: 10.1016/j.saa.2004.06.056
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Synthesis, properties and thermal studies of oxorhenium(V) complexes with 3-hydrazino-5,6-diphenyl-1,2,4-triazine, benzimidazolethione and 2-hydrazinobenzimidazole

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Cited by 20 publications
(14 citation statements)
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“…(2) The signals observed in the ranges 9.20-13.65, 7.09-10.46, and 7.08-9.97 ppm may be assigned to NH, HC=N, and aromatic protons, respectively. In case of complexes 5, 13, 14, and 15 new signals observed in the range 10.75-11.08 ppm (complexes 5 and 13), at 10.04 (complex 14), and 11.0 ppm (complex 15) that may be assigned to the coordinated OH groups of the 8-hydroxyquinoline [71] and salicylaldehyde and NH 2 group of glycine moieties [15] supporting the formation of ternary complexes. Finally, the absence of OH protons (hydrated H 2 O) may be due to their replacement by DMSO-d 6 molecules [50,65].…”
Section: H and 13 C Nmr Spectramentioning
confidence: 98%
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“…(2) The signals observed in the ranges 9.20-13.65, 7.09-10.46, and 7.08-9.97 ppm may be assigned to NH, HC=N, and aromatic protons, respectively. In case of complexes 5, 13, 14, and 15 new signals observed in the range 10.75-11.08 ppm (complexes 5 and 13), at 10.04 (complex 14), and 11.0 ppm (complex 15) that may be assigned to the coordinated OH groups of the 8-hydroxyquinoline [71] and salicylaldehyde and NH 2 group of glycine moieties [15] supporting the formation of ternary complexes. Finally, the absence of OH protons (hydrated H 2 O) may be due to their replacement by DMSO-d 6 molecules [50,65].…”
Section: H and 13 C Nmr Spectramentioning
confidence: 98%
“…Greater stability of the ligands compared with their complexes suggests a powerful intramolecular H-bonding in the ligands [81,82]. Complexes 1,6,8,14,15, and 16 were taken as representative examples for thermal analysis. The results of thermal analysis of the complexes ( Table 2) are in good agreement with the theoretical formulae as suggested from elemental analyses.…”
Section: Thermal Analysismentioning
confidence: 99%
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“…On the other hand, the bands observed in the 1503-1561 cm -1 range of the C=N (phenanthroline ring) and C=C (Ar) groups were shifted to higher frequencies in the range 1522-1577 cm -1 in all the complexes of the ligand, that indicates the participation nitrogen atom of the C=N (phenanthroline ring) groups in coordination of the metal ion [31,32].…”
Section: Ir Spectramentioning
confidence: 95%
“…The mixture was cooled. The solid obtained was filtered off and crystalized from ethanol to give yellowish crystals [18] Diffraction data of compounds 1-3 were collected on Oxford Diffraction SuperNova (single source at offset) Eos diffractometer equipped with a graphite-monochromatic CuK α radiation at 296 K. The structures were solved by direct methods using SHELXS-97 and refined by full-matrix least-squares method using SHELXL-97 [19]. All non-hydrogen atom parameters were refined anisotropically and all H atoms except for H atoms bonded nitrogen atoms were refined using a riding model with C-H distances of 0.93 Å. H atoms bonded nitrogen atoms were located in a difference map and refined freely.…”
Section: (56-diphenyl-[124]triazin-3-yl)-hydrazine (2)mentioning
confidence: 99%