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Cited by 17 publications
(10 citation statements)
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“…Thioamide band (I) is due to m(C=N) mainly and partially d(NH) + d(CH) was shifted to higher frequency on complex formation [24,25]. Thioamide band (II) which is due to m(C=S) mainly and partially m(C=N) was shifted to a lower frequency on coordination through the sulfur atom only and split into two bands, one with a lower frequency, the other with a higher frequency when ligand coordinated from both S-and N-atoms [1]. Thioamide band (III) which is mainly due to m(C-S) and partially to m(C-S) + m(C-N) was only reduced in intensity on complex formation [1].…”
Section: Ir Spectramentioning
confidence: 99%
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“…Thioamide band (I) is due to m(C=N) mainly and partially d(NH) + d(CH) was shifted to higher frequency on complex formation [24,25]. Thioamide band (II) which is due to m(C=S) mainly and partially m(C=N) was shifted to a lower frequency on coordination through the sulfur atom only and split into two bands, one with a lower frequency, the other with a higher frequency when ligand coordinated from both S-and N-atoms [1]. Thioamide band (III) which is mainly due to m(C-S) and partially to m(C-S) + m(C-N) was only reduced in intensity on complex formation [1].…”
Section: Ir Spectramentioning
confidence: 99%
“…Thioamide band (II) which is due to m(C=S) mainly and partially m(C=N) was shifted to a lower frequency on coordination through the sulfur atom only and split into two bands, one with a lower frequency, the other with a higher frequency when ligand coordinated from both S-and N-atoms [1]. Thioamide band (III) which is mainly due to m(C-S) and partially to m(C-S) + m(C-N) was only reduced in intensity on complex formation [1]. Thioamide band (IV) which is mainly due to m(C-S) was unaffected when ligands are coordinated as bidentates and shifted to a higher frequency on coordination as monodentates [24].…”
Section: Ir Spectramentioning
confidence: 99%
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