Detailed Information on Publication Record
2011
Synthesis and structure of lanthanide complexes with large-bite diphosphine dioxide ligands
SPÍCHAL, Zdeněk, Blanka VRBKOVÁ, Zdeněk MORAVEC, Jiří PINKAS, Marek NEČAS et. al.Basic information
Original name
Synthesis and structure of lanthanide complexes with large-bite diphosphine dioxide ligands
Name in Czech
Syntéza a struktura komplexů lanthanoidů s fosforanovými ligandy s dlouhým skeletem
Authors
SPÍCHAL, Zdeněk (203 Czech Republic, belonging to the institution), Blanka VRBKOVÁ (203 Czech Republic, belonging to the institution), Zdeněk MORAVEC (203 Czech Republic, belonging to the institution), Jiří PINKAS (203 Czech Republic, belonging to the institution) and Marek NEČAS (203 Czech Republic, guarantor, belonging to the institution)
Edition
Polyhedron, Velká Británie, Elsevier Science Ltd. 2011, 0277-5387
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10402 Inorganic and nuclear chemistry
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.057
RIV identification code
RIV/00216224:14310/11:00049772
Organization unit
Faculty of Science
UT WoS
000291498600024
Keywords in English
Diphosphine dioxide;Lanthanides;Coordination polymers;Chelates;X-ray crystallography
Tags
International impact, Reviewed
Změněno: 7/4/2012 14:40, Ing. Andrea Mikešková
Abstract
V originále
Three large-bite diphosphine dioxide ligands were reacted with lanthanide salts to yield either molecular or polymeric complexes. The two flexible ligands gave bischelate complexes of general formulae [Ln(dppfO2)2Clx(NO3)2-x][FeCl4] and [Ln(dppdO2)2(NO3)2]NO3, where dppfO2 and dppdO2 are bis(diphenylphosphoryl) ferrocene and bis(diphenylphosphoryl)diphenyl ether, respectively. Reactions of the rigid bis(diphenylphosphoryl)benzene (dppbO2) with lanthanide salts yielded linear coordination polymers of a 1:1.5 metal-to-ligand stoichiometry. The compounds were studied by single crystal X-ray diffraction, IR spectroscopy, mass spectrometry, and TG/DSC techniques.
Links
GA203/08/1111, research and development project |
| ||
MSM0021622410, plan (intention) |
| ||
MUNI/A/0980/2009, interní kód MU |
|