Multinuclear NMR Studies and Reaction with tert-Butyl Isocyanide of Dinuclear Tungsten- or Molybdenum-Palladium .mu.-Alkylidene Complexes. X-ray Structure of [PdI[.mu.-C(p-tolyl)dmba][.mu.-CO]Mo(Cp)(CN-t-Bu)2]

1995 ◽  
Vol 14 (4) ◽  
pp. 1637-1645 ◽  
Author(s):  
Alceo Macchioni ◽  
Paul S. Pregosin ◽  
Philippus F. Engel ◽  
Stefan Mecking ◽  
Michel Pfeffer ◽  
...  

2004 ◽  
Vol 689 (22) ◽  
pp. 3513-3519 ◽  
Author(s):  
Maria Helena Araujo ◽  
Maria D. Vargas ◽  
Anthony G. Avent ◽  
Dario Braga ◽  
Fabrizia Grepioni


Polyhedron ◽  
2007 ◽  
Vol 26 (18) ◽  
pp. 5349-5354 ◽  
Author(s):  
Iwona Łakomska ◽  
Magdalena Barwiołek ◽  
Andrzej Wojtczak ◽  
Edward Szłyk
Keyword(s):  
X Ray ◽  


Polyhedron ◽  
2007 ◽  
Vol 26 (4) ◽  
pp. 803-810 ◽  
Author(s):  
Iwona Łakomska ◽  
Andrzej Wojtczak ◽  
Jerzy Sitkowski ◽  
Lech Kozerski ◽  
Edward Szłyk
Keyword(s):  
X Ray ◽  


1993 ◽  
Vol 12 (8) ◽  
pp. 2947-2954 ◽  
Author(s):  
Maria Helena A. Benvenutti ◽  
Maria D. Vargas ◽  
Dario Braga ◽  
Fabrizia Grepioni ◽  
Brian E. Mann ◽  
...  
Keyword(s):  
X Ray ◽  




2011 ◽  
Vol 64 (12) ◽  
pp. 1583 ◽  
Author(s):  
Lili Duan ◽  
Vitaly Nesterov ◽  
Jason W. Runyon ◽  
Gregor Schnakenburg ◽  
Anthony J. Arduengo III ◽  
...  

The formation of phosphinidenoid complex salts having weakly coordinating cations (WCCs) is reported via treatment of P-functional phosphane complexes with N,N’-di-tert-butyl imidazol-2-ylidene or a P4-t-Bu phosphazene base. The thermal stability of phosphinidenoid complex salts is dependent upon the P–X substituents and the nature of the WCC. The complexes were characterized by multinuclear NMR spectroscopy and confirmed by single-crystal X-ray structure.



Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 1899
Author(s):  
Roman Franz ◽  
Clemens Bruhn ◽  
Rudolf Pietschnig

tert-Butyl-substituted diphospha[2]ferrocenophane was used as a stereochemically confined diphosphane to investigate the addition of various dichalcoganes (R2Ch2; Ch = S, Se, Te and R = Me, Ph). Bischalcogenophosphinous acid esters bearing four soft donor sides were obtained as a mixture of rac and meso diastereomers and characterized by means of multinuclear NMR and X-ray analysis. The coordination chemistry of multidentate ligand 3b was explored toward d10 coinage metal centers (Cu(I), Ag(I), and Au(I)), yielding various bimetallic complexes.



2005 ◽  
Vol 690 (21-22) ◽  
pp. 4611-4619 ◽  
Author(s):  
Maria Helena Araujo ◽  
Regina M.S. Pereira ◽  
Maria D. Vargas ◽  
Dario Braga ◽  
Fabrizia Grepioni


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