1998
DOI: 10.1016/s0379-6779(98)80100-8
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Synthesis, characterization and electrical conductivity of polyesters, polyamides and doped polymers

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Cited by 14 publications
(6 citation statements)
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“…at 1660 and 1655 cm −1 , respectively, for υ C=O of ester group and strong intensity band at 1557 and 1569 cm −1 , respectively, for υ C=C of aromatic rings. Similar assignments are reported for related Schiff bases and polyesters[10,29,31,32]. 1 HNMR spectroscopyThe 1 HNMR spectrum of diphenol Schiff base DIP indicated proton signal of OH group at δ ppm 10.568, azomethine (CH=N) proton signal at 9.781 ppm and range of CH aromatic protons signals within 5.963-7.751 ppm (Fig.S6).…”
supporting
confidence: 75%
See 1 more Smart Citation
“…at 1660 and 1655 cm −1 , respectively, for υ C=O of ester group and strong intensity band at 1557 and 1569 cm −1 , respectively, for υ C=C of aromatic rings. Similar assignments are reported for related Schiff bases and polyesters[10,29,31,32]. 1 HNMR spectroscopyThe 1 HNMR spectrum of diphenol Schiff base DIP indicated proton signal of OH group at δ ppm 10.568, azomethine (CH=N) proton signal at 9.781 ppm and range of CH aromatic protons signals within 5.963-7.751 ppm (Fig.S6).…”
supporting
confidence: 75%
“…Two new Schiff bases 4,4′-diphenylsulfonebis(p-iminomethylphenol) (DIP) and 1,2-cyclohexanebis(p-iminomethylphenol) (CIP) were synthesized through condensation reaction by following a reported general procedure [29] with slight modification. 0.01 mol of diamine (4,4′-diaminodiphenyl sulfone (dapsone) or 1,2-cyclohexanediamine) was dissolved in 100 mL absolute ethanol and then transferred in a 250-mL round-bottom flask.…”
Section: Synthesis Of Diphenol Schiff Basesmentioning
confidence: 99%
“…In addition, the appearance of new band at 335 cm −1 showing the involvement of M-Cl bond in complex formation, supporting the IR spectral study. Further conclusive evidence of coordination of the Schiff base with the metal ion was shown by the appearance of low frequency new band at 648 cm −1 due to metal-oxygen ] (M-O) vibrations [25,26] and was observed in the spectra of the thus confirming participation of the oxygen atom in the coordination. Further coordination of metal to azomethine nitrogen is confirmed by a new band at 508 cm −1 with the involvement of the imidazole ring nitrogen in the coordination with metal ion [27] due to ] (M-N) .…”
Section: Ir Spectral Studymentioning
confidence: 91%
“…This band is absent in all the metal complexes indicating the involvement of this group in complex formation [23]. Moreover, the shift of the C-O phenolic bands from 1282 cm −1 in ligand to 1282-1312 cm −1 in the spectra of metal complexes supports the coordination of the phenolic oxygen atom to the metal ion [24]. The bands for M-O modes appeared in the range of 580 cm −1 -615 cm −1 in all the complexes [25].…”
Section: Spectral Studies Of Ligand and Its Complexesmentioning
confidence: 96%