Thermodynamic properties of bis-(η6-cumene)chromium fulleride [(η6-PhCH(CH3)2)2Cr].+[C60].- over the range from T → (0 to 310) K

被引:5
|
作者
Markin, A. V. [1 ]
Ruchenin, V. A. [1 ]
Smirnova, N. N. [1 ]
Abakumov, G. A. [2 ]
Markin, G. V. [2 ]
Shevelev, Yu. A. [2 ]
Kuropatov, V. A. [2 ]
Lopatin, M. A. [2 ]
Cherkasov, V. K. [2 ]
Domrachev, G. A. [2 ]
机构
[1] Nizhnii Novgorod State Univ, Inst Chem, Nizhnii Novgorod 603950, Russia
[2] Russian Acad Sci, Razuvaev Inst Organometall Chem, Nizhnii Novgorod 603950, Russia
来源
JOURNAL OF CHEMICAL THERMODYNAMICS | 2011年 / 43卷 / 10期
关键词
Bis-(eta(6)-cumene)chromium fulleride; Precise adiabatic calorimetry; Heat capacity; Standard thermodynamic functions; SOLID C-60; POLYMERIZATION; TRANSITION; PHASES; DIMER;
D O I
10.1016/j.jct.2011.05.005
中图分类号
O414.1 [热力学];
学科分类号
摘要
In the present research, the temperature dependence of heat capacity C-p,m(o) = f(T) of crystalline bis-(eta(6)-cumene)chromium fulleridel [(eta(6)-PhCH(CH3)(2))(2)Cr](.+)[C-60](.-) has been measured between T = (6 and 310) K in the precision adiabatic vacuum calorimeter and reported for the first time. Also, for the first time, the temperature dependence of EPR signal parameters of bis-(eta(6)-cumene)chromium fulleride over the range from T = (120 to 290) K was investigated by electron paramagnetic resonance. In the interval from T = (196 to 240) K the reversible endothermic transformation was detected and its thermodynamic characteristics were estimated. This transformation was caused by dissociation of dimer (C-60(-))(2) and formation of fulleride [(eta(6)-PhCH(CH3)(2))(2)Cr](.+)[C-60](.-) during heating. The experimental results have been used to calculate the standard (p(o) = 0.1 MPa) thermodynamic functions C-p,m(o)/R, Delta H-T2(T1)m(o)/RT, Delta S-T2(T1)m(o)/R, and Phi(o)(m)/R = Delta S-T2(T1)m(o)/R - Delta H-T2(T1)m(o)/RT (where R is the universal gas constant) for dimeric fulleride over the range from T (0 to 196) K and for monomeric complex [(eta(6)-PhCH(CH3)(2))(2)Cr](.+)[C-60](.-) between T = (240 and 310) K. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1495 / 1499
页数:5
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