Infrared Spectra and Electronic Structure Calculations for the NUN(NN)1-5 and NU(NN)1-6 Complexes in Solid Argon

被引:19
作者
Andrews, Lester [1 ,2 ]
Wang, Xuefeng [1 ,2 ]
Gong, Yu [1 ,2 ]
Vlaisavljevich, Bess [3 ,4 ]
Gagliardi, Laura [3 ,4 ]
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA
[2] Tongji Univ, Dept Chem, Shanghai 200093, Peoples R China
[3] Univ Minnesota, Dept Chem, Supercomp Inst, Minneapolis, MN 55455 USA
[4] Univ Minnesota, Chem Theory Ctr, Minneapolis, MN 55455 USA
关键词
URANIUM ATOMS; REACTION-PRODUCTS; BOND ORDER; DIHYDRIDE; MOLECULES; NITRIDE;
D O I
10.1021/ic401857u
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reactions of laser-ablated U atoms with N-2 molecules in excess argon during co-deposition at 4 K gave intense NUN and weaker UN absorptions. Annealing increased progressions of new absorptions for the NUN(NN)(1,2,3,4,5) and NU(NN)(1,2,3,4,5,6) uranium nitride complexes. Small matrix shifts are observed when the secondary coordination layers around the primary NUN(NN)(1,2,3,4,5) and NU(NN)(1,2,3,4,5,6) complexes are changed from argon to *nitrogen: Electronic structure and energy and frequency calculations provide support for the identification of these complexes and further characterization of the N equivalent to U equivalent to N and UN core molecules as terminal uranium nitrides with full triple bonds.
引用
收藏
页码:9989 / 9993
页数:5
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