Premium
Hydrothermal Synthesis and Characterization of Novel Lanthanide 2,2′‐Diphenyldicarboxylate Complexes
Author(s) -
Wang YiBo,
Zheng XiangJun,
Zhuang WenJuan,
Jin LinPei
Publication year - 2003
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200390175
Subject(s) - lanthanide , isostructural , chemistry , crystallography , hydrothermal synthesis , hydrothermal circulation , zigzag , crystal structure , ion , single crystal , diffraction , stereochemistry , geometry , organic chemistry , physics , mathematics , optics , seismology , geology
Lanthanide complexes with a one‐dimensional chain, [Ln 2 (dpdc) 3 (H 2 O) 2 ] n [Ln = La ( 1 ), Pr ( 2 ), Eu ( 3 ), Tb ( 4 ); dpdc = 2,2′‐diphenyldicarboxylate] were obtained by hydrothermal reaction of lanthanide( III ) chlorides and 2,2′‐diphenyldicarboxylic acid, and characterized by X‐ray diffraction. The crystal structure data reveal that they are isostructural. In the asymmetric unit, the two Ln 3+ ions are both eight‐coordinate but they have different coordination environments. Lanthanide ions arranged in a zigzag manner are bridged by the dpdc ligands into a 1‐D chain, while the structure appears like a pinwheel viewed along the c axis. In these complexes, 2,2′‐diphenyldicarboxylate anions exhibit tetradentate and pentadentate coordination modes. A laser‐induced highresolution spectrum (resolution: 0.2 cm −1 ) of 3 was obtained, which shows two Eu 3+ sites in 3 . This is in agreement with the results of single‐crystal X‐ray diffraction studies of 3 . (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom