Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Thermochemistry of 2,2,6,6-tetramethyl-3,5-heptanedione chelates of lanthanide group elements
Author: Santos, LS
Petrucelli, GP
Airoldi, C
Abstract: Solution-reaction calorimetry was used to determine the standard molar (p'=0.10 Mpa) enthalpies of formation of crystalline chelates Ln(thd)(3) (Ln=Nd, Sm, Gd, Tb, Er, Tm, Yb, Lu and thd=2,2,6,6-tetramethyl-3,5-heptanedionate), at (T=298.15+/-0.02) K, to give: 4054+/-1.21; 37.77+/-1.78; 8.06+/-0.80; 26.43+/-1.61; 51.05+/-1.10; 66.75+/-1.30; 50.39+/-1.64 and 39.00+/-1.33 kJ mol(-1), respectively. The corresponding molar enthalpies of sublimation 159.1+/-3.4; 149.7+/-3.4; 166.1+/-3.5; 138.4+/-2.6; 130.8+/-2.2; 131.3+/-2.9; 131.1+/-2.7 and 135.8+/-2.9 kJ mol(-1) were obtained by means of differential scanning calorimetry. From the standard molar enthalpies of dissociation of the chelates 1518+/-62; 1405+/-62; 1605+/-62; 1599+/-62; 1525+/-62; 1408+/-62; 1333+/-62; and 1720+/-62 kJ mol(-1), respectively, the mean lanthanide-oxygen bond dissociation enthalpies were also calculated to be 253+/-10; 234+/-10; 268+/-10; 266+/-10; 254+/-10; 235+/-10; 222+/-10 and 287+/-10 kJ mol(-1), by assuming the equivalence of all bonds in the chelates. This last value correlated with the atomic number of the metal elements to give an inclined W, proposed to systematize lanthanide properties, also indicating that the nature of the coordination established on lanthanide is very close to that found in the respective lanthanide oxides. (C) 1999 Elsevier Science Ltd. All rights reserved.
Subject: lanthanide
lanthanide-oxygen bond
Country: Inglaterra
Editor: Pergamon-elsevier Science Ltd
Citation: Polyhedron. Pergamon-elsevier Science Ltd, v. 18, n. 7, n. 969, n. 977, 1999.
Rights: fechado
Identifier DOI: 10.1016/S0277-5387(98)00380-5
Date Issue: 1999
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
WOS000080231900006.pdf166.87 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.