Synthesis, Solid-State Structure and Multinuclear NMR Studies of the New Polyhydrido Iridium Carbonyl Cluster Ir4H4(μ-H)4(CO)4(PPh3)4

2003 ◽  
Vol 2003 (11) ◽  
pp. 2108-2112 ◽  
Author(s):  
Luigi Garlaschelli ◽  
Francesco Greco ◽  
Giulia Peli ◽  
Mario Manassero ◽  
Mirella Sansoni ◽  
...  
2011 ◽  
Vol 18 (4) ◽  
pp. 1168-1179 ◽  
Author(s):  
Fabian Dielmann ◽  
Andrea Schindler ◽  
Sabine Scheuermayer ◽  
Junfeng Bai ◽  
Roger Merkle ◽  
...  

1994 ◽  
Vol 5 (2) ◽  
pp. 363-371 ◽  
Author(s):  
Roberto Della Pergola ◽  
Elisa Brivio ◽  
Luigi Garlaschelli ◽  
Norberto Masciocchi ◽  
Mario Manassero

2000 ◽  
Vol 78 (4) ◽  
pp. 454-458 ◽  
Author(s):  
David J Berg ◽  
Roland AL Gendron

The synthesis of [Ln{N(SiMe3)2}2(THF)(µ-Cl)]2 (Ln = Ce, 1; Nd, 2) by reaction of sodium bis(trimethylsilyl)amide (2 equiv.) with LnCl3 is reported. The same complexes were also isolated from the ligand redistribution reactions of Ln[N(SiMe3)2]3 and LnCl3 (2:1 ratio) in THF at 80°C. The crystal structure of 2, determined by X-ray diffraction, revealed a centrosymmetric dimer with bridging chlorides and pentacoordinate metal centres. 1H NMR studies show that the solid state structure is not maintained in solution. NMR evidence for the presence of Ln[N(SiMe3)2]3 and two other bis(trimethylsilyl)amide containing species, presumably Ln[N(SiMe3)2]Cl2(THF)x and Ln[N(SiMe3)2]2Cl(THF)y, is presented.Key words: lanthanide, amide, neodymium, cerium, crystal structure, X-ray, nuclear magnetic resonance, redistribution.


2014 ◽  
Vol 69 (11-12) ◽  
pp. 1269-1289 ◽  
Author(s):  
Bernd Wrackmeyer ◽  
Elena V. Klimkina ◽  
Wolfgang Milius ◽  
Christian Butterhof ◽  
Kathrin Inzenhofer

Abstract Alkynyl(ferrocenyl)vinylsilanes containing up to three alkynyl units were prepared and treated with 9-borabicyclo[3.3.1]nonane (9-BBN). All reactions proceeded in the beginning by regioselective 1,2-hydroboration of the vinyl group, with boron attached to the terminal carbon. This was followed by intra-molecular 1,1-carboboration, leading to fused silacarbacycles, depending on the number of C≡C bonds. Thus, new siloles and even fused siloles became available. The solution-state structures were revealed by multinuclear NMR techniques (1H, 11B, 13C, 29Si NMR), complemented by calculated single-molecule structures and calculated NMR parameters at the B3LYP/6-311+G(d,p) level of theory. In one case, the solid-state structure of a bicyclic derivative was determined.


2004 ◽  
Vol 2004 (21) ◽  
pp. 4452-4466 ◽  
Author(s):  
Rosa M. Claramunt ◽  
Dionisia Sanz ◽  
Marta Pérez-Torralba ◽  
Elena Pinilla ◽  
M. Rosario Torres ◽  
...  

2008 ◽  
Vol 59 (11) ◽  
Author(s):  
Mircea Braban ◽  
Ionel Haiduc

The paper describes the solid state structure of a compound of composition [Cu(bipy)3][Cu(bipy)(ala) (ClO4)2]ClO4, in which both the cation and anion are octahedral complex species with copper(II) as coordination center. The cation contains three chelate rings formed by bipy; the anion contains in the quatorial plane a CuONC2 chelate ring formed by the alaninato ligand and a CuN2C2 chelate ring formed by bipy, with two monodentate perchorato ligands in axial positions completing the six-coordination. In the crystal p-p stackings lead to a supramolecular self-assembled structure.


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