Bhattacharya Sumanta, Banerjee Shrabanti, Nayak Sandip K, Chattopadhyay Subrata, Mukherjee Asok K
Department of Chemistry, University of Burdwan, Golapbag, Burdwan 713104, India.
Spectrochim Acta A Mol Biomol Spectrosc. 2004 Apr;60(5):1099-104. doi: 10.1016/S1386-1425(03)00343-3.
Molecular complex formation between [60]- and [70]fullerenes with a series of phosphine oxides, namely, tri-n-octyl phosphine oxide, triphenyl phosphine oxide and tri-n-butyl phosphine oxide has been studied in CCl4 medium by NMR spectrometric method. Both [60]- and [70]fullerenes have been shown to form 1:1 adducts with the above series of phosphine oxides. Formation constants (K) for all the complexes have been determined from the systematic variation of NMR chemical shifts of specific protons of the donors in presence of [60]- and [70]fullerenes. Trends in the values of K suggest that [70]fullerene binds stronger with the phosphine oxides relative to [60]fullerene.
通过核磁共振光谱法,在四氯化碳介质中研究了[60]富勒烯和[70]富勒烯与一系列氧化膦(即三正辛基氧化膦、三苯基氧化膦和三正丁基氧化膦)之间的分子复合物形成。结果表明,[60]富勒烯和[70]富勒烯均与上述系列氧化膦形成1:1加合物。根据在[60]富勒烯和[70]富勒烯存在下供体特定质子的核磁共振化学位移的系统变化,确定了所有复合物的形成常数(K)。K值的趋势表明,相对于[60]富勒烯,[70]富勒烯与氧化膦的结合更强。