Synthesis and reactivity of side-on-bound dinitrogen metal complexes

被引:124
作者
MacLachlan, EA [1 ]
Fryzuk, MD [1 ]
机构
[1] Univ British Columbia, Dept Chem, Vancouver, BC V6T 1Z1, Canada
关键词
D O I
10.1021/om051055i
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
An up-to-date account of the Synthesis of side-on-bound dinitrogen complexes of the lanthanides, the actinides, and the transition elements over the past 40 years is given. In addition, the reactivity of these derivatives is summarized. There have been many complicated multinuclear Cluster complexes with the N-2 imbedded in a fashion that corresponds to side-on N-2. There have been some suggestions, as early as 1960. that side-on dinitrogen complexes should exist. However, a key date in this area is 1988, which is when the disamarium Complex (CP*Sm-2)(2)(mu-eta(2):eta(2)-N-2) was reported. It is this date that is used in this account as the real starting point for the area of side-on dinitrogen coordination chemistry. After 1988, side-on dinitrogen complexes are reviewed from the point of view of Synthesis, structure (N-N bond lengths, where applicable), and reactivity. What becomes apparent is that while there have been many new side-on dinitrogen complexes discovered recently, investigations into their reactivity patterns are still at a primitive stage.
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页码:1530 / 1543
页数:14
相关论文
共 112 条
[1]   NITROGENOPENTAMMINERUTHENIUM(2) COMPLEXES [J].
ALLEN, AD ;
SENOFF, CV .
CHEMICAL COMMUNICATIONS, 1965, (24) :621-&
[2]   LINKAGE ISOMERIZATION IN NITROGEN-LABELED RU(NH3)5N2!BR2 [J].
ARMOR, JN ;
TAUBE, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1970, 92 (08) :2560-+
[3]  
ARNAUDET L, 1983, CR ACAD SCI II, V296, P431
[4]   Why does the reaction of the dihydrogen molecule with [P2N2]Zr(μ-η2-N2)Zr[P2N2] produce [P2N2]Zr(μ-η2-N2H)Zr[P2N2](μ-H) but not the thermodynamically more favorable [P2N2]Zr(μ-NH)2Zr[P2N2]?: A theoretical study [J].
Basch, H ;
Musaev, DG ;
Morokuma, K .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (24) :5754-5761
[5]   Call the binuclear dinitrogen complex [P2N2]Zr(μ-η2-N2)Zr[P2N2] activate more than one hydrogen molecule?: A theoretical study [J].
Basch, H ;
Musaev, DG ;
Morokuma, K .
ORGANOMETALLICS, 2000, 19 (17) :3393-3403
[6]   Theoretical predictions and single-crystal neutron diffraction and inelastic neutron scattering studies on the reaction of dihydrogen with the dinuclear dinitrogen complex of zirconium [P2N2]Zr(μ-η2-N2)Zr[P2N2], P2N2=PhP(CH2SiMe2NSiMe2CH2)2PPh [J].
Basch, H ;
Musaev, DG ;
Morokuma, K ;
Fryzuk, MD ;
Love, JB ;
Seidel, WW ;
Albinati, A ;
Koetzle, TF ;
Klooster, WT ;
Mason, SA ;
Eckert, J .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (03) :523-528
[7]   N2 hydrogenation promoted by a side-on bound hafnocene dinitrogen complex [J].
Bernskoetter, WH ;
Olmos, AV ;
Lobkovsky, E ;
Chirik, PJ .
ORGANOMETALLICS, 2006, 25 (04) :1021-1027
[8]   Kinetics and mechanism of N2 hydrogenation in bis(cyclopentadienyl) zirconium complexes and dinitrogen functionalization by 1,2-addition of a saturated C-H bond [J].
Bernskoetter, WH ;
Lobkovsky, E ;
Chirik, PJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (40) :14051-14061
[9]   Dinitrogen functionalization with terminal alkynes, amines, and hydrazines promoted by [(η5-C5Me4H)2Zr]2(μ2,η2 η2-N2):: Observation of side-on and end-on diazenido complexes in the reduction of N2 to hydrazine [J].
Bernskoetter, WH ;
Pool, JA ;
Lobkovsky, E ;
Chirik, PJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (21) :7901-7911
[10]   Serendipitous isolation of the first example of a mixed-valence samarium tripyrrole complex [J].
Bérubé, CD ;
Yazdanbakhsh, M ;
Gambarotta, S ;
Yap, GPA .
ORGANOMETALLICS, 2003, 22 (18) :3742-3747