1979
DOI: 10.1021/ic50199a040
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Carbon-13 nuclear magnetic resonance study of coordinated thiocyanate, selenocyanate, and cyanate

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Cited by 58 publications
(70 citation statements)
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“…The resonance signal is slightly shielded as compared to that of the free NCO anion at d 131.1 (NaNCO in D 2 O in a sealed capillary), also supporting the N-coordination of the isocyanate ligand in 3. This observation is consistent with the previous report demonstrating that the 13 C resonance signals of the isocyanate ligands upon coordination through nitrogen (MeNCO) shift to upfield, slightly, as compared to that of the free NCO anion [78].…”
Section: Azido and Isocyanato Complexes: Reaction Of The Azide With Cosupporting
confidence: 93%
“…The resonance signal is slightly shielded as compared to that of the free NCO anion at d 131.1 (NaNCO in D 2 O in a sealed capillary), also supporting the N-coordination of the isocyanate ligand in 3. This observation is consistent with the previous report demonstrating that the 13 C resonance signals of the isocyanate ligands upon coordination through nitrogen (MeNCO) shift to upfield, slightly, as compared to that of the free NCO anion [78].…”
Section: Azido and Isocyanato Complexes: Reaction Of The Azide With Cosupporting
confidence: 93%
“…Signals at 119 ppm for selenocyanato carbon represent its N-bonded coordination. All the 13 C shifts are consistent with results for complex 1 for the observed mode of bonding in a number of inorganic and organic complexes [29][30][31].…”
Section: Nmr Spectrasupporting
confidence: 86%
“…2140 cm À1 for alkyl thiocyanates [20]) and 13 C NMR, spectroscopy (7, -S-CN, d = 110.16 ppm, cf. d = 112.1 and 127.8 ppm for C 2 H 5 SCN and C 2 H 5 NCS, respectively [21,22]). Interestingly, compound 7 has significantly higher stability compared to compound 5.…”
Section: And Thiocyanates Saltsmentioning
confidence: 99%
“…However, when the reaction of 2 and phenyl isothiocyanate (22) was carried out in the presence of tetrabutylammonium fluoride catalyst, it resulted in high yield formation of imine 22a (Scheme 13).…”
Section: Reactions Of Epoxides 1 and 2 With Aryl- Fluoroalkenylisothmentioning
confidence: 99%