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'13 C CP MAS NMR' in keywords
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1998 (1)
1996 (1)
1Author    Takahiro Ueda, Katsuyuki Shimizu, Hiroshi Ohki, Tsutomu OkudaRequires cookie*
 Title    C CP/MAS NMR Study of Motion and Local Structure of Phenethyl- ammonium Ion in [C 6 H 5 CH 2 CH 2 NH 3 ] 2 PbX 4 (X = Cl, Br, I)  
 Abstract    Ionic motion and local structure of phenethylammonium ion (C 6 H 5 CH-,CH 2 NH 3 +) in a series of phenethylammonium lead(II) halides, [C 6 H 5 CH 2 CH 2 NH 3 ] 2 PbX 4 (X = Cl, Br, I) were studied by means of 13 C cross polarization/magic angle sample spinning (CP/MAS) NMR technique. Among the three salts, remarkable differences in the spectra were observed in the signals corresponding to the phenyl carbons. The peaks from C2, C3, C5, and C6 in the phenyl group were split into three for the chloride and into two for the bromide, although in the iodide those were observed as a single peak. Coalescence of those peaks, as well as line broadening were observed on heating. This indicated that peak split brings about disorder of the orientation in the phenyl group around the C1-C4 axis, suggesting to have three and two orientations for the chloride and the bromide, respectively. Above room temperature the phenyl group undergoes chemical exchange among these orientations, and at higher temperature, reorientation with a large amplitude takes place around its axis. The apparent activation energies of the reorientation of the phenyl group for the chloride and bromide were estimated from the temperature dependence of the linewidth of the resonance peaks to be about 24 kJ mol -1 , 25 kJ mol -1 , respectively, which is similar to in the iodide (25.0 kJ mol -1). Ab initio molecular orbital energy calculation was carried out to evaluate the potential barrier of the internal rotation of the phenyl group in a free phenethylammonium ion. The intramolecular interaction was evaluated to be 13.9 kJ mol -1 from the calculation, and the intermolecular interaction results to be 10 kJmol -1 . 
  Reference    Z. Naturforsch. 53a, 983—988 (1998); received April 30 1998 
  Published    1998 
  Keywords    13 C CP/MAS NMR, Layered compound, Disorder, Reorientation, Activation energy 
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 TEI-XML for    default:Reihe_A/53/ZNA-1998-53a-0983.pdf 
 Identifier    ZNA-1998-53a-0983 
 Volume    53 
2Author    T. Ueda, K. Shimizu, H. Ohki, T. OkudaRequires cookie*
 Title    C CP/MAS NMR Study of the Layered Compounds [C 6 H 5 CH 2 CH 2 NH3] 2 [CH 3 NH 3 ] fI _ 1 Pb n l3 n+1 (n = 1, 2)  
 Abstract    19, 1996 13 C CP/MAS NMR spectra were measured on the layered compounds [C 6 H 5 CH 2 CH 2 NH 3 ] 2 [CH 3 NH 3 ] n _ 1 Pb"I 3n + j (w = 1, 2). The linewidth of the resonance peak corresponding to the phenyl carbons changed with temperature. The maximum broadening took place at 363 K for both com-pounds. The activation energy £ a for the reorientation of the phenyl group was determined to be 25 kJ mol" 1 for n — 1 and 26 kJ mol" 1 for n = 2. The frequency factor t 0 was evaluated from the linewidth at 363 K. The value of the second moment, estimated from the maximum linewidth, was interpreted by assuming a 180° flip of the phenyl group around its two-fold axis. The similarity of the activation energies for the reorientation of the phenyl group suggested that the local structure and the molecular motion of the organic cations is little affected by the difference in the sub-structure of the inorganic layer in those compounds. 
  Reference    Z. Naturforsch. 51a, 910—914 (1996); received March 
  Published    1996 
  Keywords    13 C CP/MAS NMR, Molecular motion, Layered compounds Activation parameters, Local structure 
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 TEI-XML for    default:Reihe_A/51/ZNA-1996-51a-0910.pdf 
 Identifier    ZNA-1996-51a-0910 
 Volume    51