2015
DOI: 10.1016/j.molstruc.2015.08.019
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1D cyanide complexes with 2-pyridinemethanol: Synthesis, crystal structures and spectroscopic properties

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Cited by 10 publications
(4 citation statements)
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“…1430 cm −1 can be assigned to the δ (CH 2 ) deformation mode. Compared with 2 a – c , the asymmetric ν (CH 2 ) stretching and δ (CH 2 ) deformation vibrations are shifted slightly to higher frequencies ( 2 a – c , 2903/2853 and 1434 cm −1 ) [63] . The C−N unit of the Py ligands gives rise to bands at 1594 and 1572 cm −1 ( 3 a ), 1595 and 1579 cm −1 ( 3 b ), as well as 1605 cm −1 ( 3 c ) ( ν (C=N)), and at 1260 cm −1 ( 3 a ), 1229 cm −1 ( 3 b ) and 1220 cm −1 ( 3 c ) ( ν (C−N)).…”
Section: Resultsmentioning
confidence: 89%
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“…1430 cm −1 can be assigned to the δ (CH 2 ) deformation mode. Compared with 2 a – c , the asymmetric ν (CH 2 ) stretching and δ (CH 2 ) deformation vibrations are shifted slightly to higher frequencies ( 2 a – c , 2903/2853 and 1434 cm −1 ) [63] . The C−N unit of the Py ligands gives rise to bands at 1594 and 1572 cm −1 ( 3 a ), 1595 and 1579 cm −1 ( 3 b ), as well as 1605 cm −1 ( 3 c ) ( ν (C=N)), and at 1260 cm −1 ( 3 a ), 1229 cm −1 ( 3 b ) and 1220 cm −1 ( 3 c ) ( ν (C−N)).…”
Section: Resultsmentioning
confidence: 89%
“…[44,59,60,62] The IR spectra of 3 a-c show vibrations representative for mono-substituted pyridyls (Experimental, for spectra see the ESI). [63] The ν(CH) stretching vibrations of the compounds can be found at 3100-3000 cm À 1 , while the asymmetric and symmetric ν(CH 2 ) bands appear at 2880-2950 cm À 1 (Experimental). The absorptions at ca.…”
Section: Resultsmentioning
confidence: 99%
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“…In this regard, the characterization of IR-786 in the absence and presence of individual anions and both anions were carried out by FT-IR ( Figure 6 ) and NMR spectroscopy (data presented in the Materials and Methods section). The FT-IR spectrum of solid IR-786 has characteristic peaks for aromatic groups between 2800 and 2980 cm −1 and lacks two important bands (–CN: 2200 cm −1 and OH: 3224 cm −1 ) due to the absence of these groups in the molecule [ 26 , 27 ]. A strong peak for –CN at 2200 cm −1 appeared when IR-786 is dissolved in MeCN and CN − is added and the aromatic peaks at 2800–2990 cm −1 became stronger due to the conversion of aromatic rings to aliphatic groups.…”
Section: Resultsmentioning
confidence: 99%