scholarly journals Infrared Spectra of the Ices at ≈4 K and the Interpretation of the v OD(D2O) Bands of Ices II and IX

1978 ◽  
Vol 21 (85) ◽  
pp. 694
Author(s):  
F. E. Bates ◽  
S. M. Jacobs ◽  
J. E. Bertie

Abstract We have studied the infrared absorption by the OD stretching, v OD(D2O), and D2O rotational, v R(D2O), vibrations of fully deuterated ice II and ice IX at lo K, and the absorption by OD stretching vibrations, v OD (HDO), of HDO molecules isolated in ices Ih, II, and IX at 10 K. Calculations of the frequencies and relative intensities of the zero-wave-vector normal v OD(D2O) vibrations of ices II and IX have allowed the v OD(D2O) absorption to be assigned. Each component of the band is broad, even at 10 K, most probably because of Fermi resonance between the fundamental OD stretching vibrational states and the isoenergetic continuum of high-order overtone and combination states of the lattice modes. This work has yielded the most complete interpretation yet achieved of an infrared band due to the OH or OD stretching vibrations of a phase of ice. The far-infrared absorption by the translational vibrations of H2O and D2O ices Ih and Ic at 4.3 K has been measured, and has revealed differences between the spectra of ices III and Ic for the first time. Papers describing this work in full have been published in Journal of Chemical Physics, Vol. 67, No. 4, 1977, p. 1311-18, and Vol. 67, No. 6, 1977, p. 2445-48.

1978 ◽  
Vol 21 (85) ◽  
pp. 694-694
Author(s):  
F. E. Bates ◽  
S. M. Jacobs ◽  
J. E. Bertie

AbstractWe have studied the infrared absorption by the OD stretching, vOD(D2O), and D2O rotational, vR(D2O), vibrations of fully deuterated ice II and ice IX at lo K, and the absorption by OD stretching vibrations, vOD (HDO), of HDO molecules isolated in ices Ih, II, and IX at 10 K. Calculations of the frequencies and relative intensities of the zero-wave-vector normal vOD(D2O) vibrations of ices II and IX have allowed the vOD(D2O) absorption to be assigned. Each component of the band is broad, even at 10 K, most probably because of Fermi resonance between the fundamental OD stretching vibrational states and the isoenergetic continuum of high-order overtone and combination states of the lattice modes. This work has yielded the most complete interpretation yet achieved of an infrared band due to the OH or OD stretching vibrations of a phase of ice.The far-infrared absorption by the translational vibrations of H2O and D2O ices Ih and Ic at 4.3 K has been measured, and has revealed differences between the spectra of ices III and Ic for the first time.Papers describing this work in full have been published in Journal of Chemical Physics, Vol. 67, No. 4, 1977, p. 1311-18, and Vol. 67, No. 6, 1977, p. 2445-48.


1970 ◽  
Vol 25 (2) ◽  
pp. 139-141 ◽  
Author(s):  
S. P. Tandon ◽  
P. C. Mehta

Infrared absorption spectra of some four- and five-coordinated (ethyl 1-methyl acetoacetate) complexes of trivalent samarium have been studied in the region 4000 - 250 cm-1 for the first time. About twenty bands in each chelate have been observed and assigned to different modes of vibration. A study of relative frequency shifts of CO stretching vibrations reveals that the metal-oxygen bonds in all the complexes are nearly of the same strength. The vibrational frequencies, with few exceptions, are found to be nearly independent of the coordination number of the metal.


1970 ◽  
Vol 25 (2) ◽  
pp. 142-145 ◽  
Author(s):  
S. P. Tandon ◽  
P. C. Mehta ◽  
R. N. Kapoor

Infrared absorption spectra of four (ethylbenzoyl acetate) [EBA] complexes of trivalent samarium of the general formula XpSm(EBA)q [X = isopropoxy or t-butoxy group; when p=1, q=2 and vice versa] have been studied in the region 4000-250 cm-1 for the first time. About twenty five bands in each complex have been observed and assigned to different modes of vibration. The separation between asymmetric and symmetric CO stretching vibrations indicates that the bonding in all the complexes is nearly the same. The spectra show that the interaction between the two ligand rings is small in five coordinated metal complexes.


1965 ◽  
Vol 14 (4) ◽  
pp. 271-273 ◽  
Author(s):  
A.J. Sievers ◽  
C.D. Lytle

1970 ◽  
Vol 5 (3) ◽  
pp. 203-206 ◽  
Author(s):  
T.A. Richter ◽  
M.L. Malhotra ◽  
K.D. Möller

1974 ◽  
Vol 27 (1) ◽  
pp. 87 ◽  
Author(s):  
ME Bridson ◽  
WR Walker

The following cobalt(11) complexes containing the chelate 2,2'-dithiodipyridine (αdtp) and the isomeric chelate 4,4'-dithiodipyridine (γdtp)* have been prepared and investigated: Co(αdtp)X2 (X = Cl, Br,I and NCS), Co(γdtp)Cl2 and Co(γdtp)2X2 (X = I and NCS). All, except the first three, are described for the first time. Physicochemical investigations indicate that the complexes Co(αdtp)X2 (X = Cl,Br and I) are tetrahedral monomers and Co(αdtp)(NCS)2 is an octahedral polymer. Co(γdtp)Cl2, appears to be tetrahedral whereas Co(γdtp)2X2 (X = I and NCS) are octahedral polymers. Although the complete interpretation of the spectra is rendered difficult by the ligand bands occurring at lowfrequencies, far-infrared spectra have provided evidence that both nitrogen atoms in αdtp and γdtp are coordinated in these complexes.


1977 ◽  
Vol 38 (C2) ◽  
pp. C2-93-C2-96 ◽  
Author(s):  
C. G. GRANQVIST ◽  
R. A. BUHRMAN ◽  
J. WYNS ◽  
A. J. SIEVERS

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