Functionalization of N2 by Mid to Late Transition Metals via N-N Bond Cleavage

被引:54
|
作者
Klopsch, Isabel [1 ]
Yuzik-Klimova, Ekaterina Yu [1 ]
Schneider, Sven [1 ]
机构
[1] Univ Goettingen, Inst Inorgan Chem, Tammannstr 4, D-37077 Gottingen, Germany
来源
NITROGEN FIXATION | 2017年 / 60卷
关键词
Bonding; Dinitrogen splitting; Nitrogen fixation; Transition metal nitrides; 3-COORDINATE MOLYBDENUM(III) COMPLEXES; DITANTALUM DINITROGEN COMPLEX; NITROGEN ATOM-TRANSFER; RAY CRYSTAL-STRUCTURE; SIDE-ON; END-ON; REDUCTIVE CLEAVAGE; X-RAY; ELECTRONIC-STRUCTURE; CATALYTIC-REDUCTION;
D O I
10.1007/3418_2016_12
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This review focuses on the recent efforts to functionalize dinitrogen via complete cleavage of the N N bond with particular emphasis on mid to late transition metal complexes. The relationships of electronic and structural parameters for the most common N-2-bonding modes (end-on and side-on bridging) with N-2-splitting reactivity are discussed. This analysis points towards electronic configurations with pi(10) (end-on) and pi(8)delta(2) (side-on) electrons within the M2N2-cores for full N-N bond cleavage into terminal and bridging nitride complexes, respectively. The full body of work on N-2-splitting with group 6-8 metals is comprehensively presented. Ligand electronic and steric effects are discussed in detail for privileged platforms, such as low coordinate, electron rich complexes with pi-donating ligands. Finally, several strategies for functionalization of the nitrides resulting from N-2-splitting are presented that lead to N-C bond formation. The developed pseudocatalytic cycles reported so far that combine N-2-cleavage, nitride functionalization, and N-transfer provide guidelines for rational catalyst design.
引用
收藏
页码:71 / 112
页数:42
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