A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
METAL COMPLEXES OF AN AMINE BISPHENOL WITH A THIOPHENE SIDE-ARM
Tekijät: Salminen E, Sillanpaa R, Lehtonen A
Kustantaja: INST ORGANIC CHEM AND BIOCHEM
Julkaisuvuosi: 2010
Journal: Collection of Czechoslovak Chemical Communications
Tietokannassa oleva lehden nimi: COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS
Lehden akronyymi: COLLECT CZECH CHEM C
Numero sarjassa: 10
Vuosikerta: 75
Numero: 10
Aloitussivu: 1051
Lopetussivu: 1060
Sivujen määrä: 10
ISSN: 0010-0765
DOI: https://doi.org/10.1135/cccc2010049
Tiivistelmä
Dioxomolybdenum(VI) and oxotungsten(VI) complexes with a new amine bisphenol ligand (H(2)L) are reported. The ligand which carries a neutral nitrogen atom, two phenolic oxygen atoms and a thiophene side-arm was synthesized by a simple one-pot Mannich reaction. Further reaction with [MoO(2)(acac)(2)] yielded a monomeric molybdenum complex [MoO(2)(L)(MeOH)] (2a) or a dimeric complex [Mo(2)O(2)(mu-O)(2)(L)(2)] (2b), depending on the reaction conditions. The reaction with a tungsten trisglycolate [W(eg)(3)] led to the formation of a monomeric compound [WO(eg)(L)] (3). In these complexes, the potentially tetradentate amine bisphenolate dianion coordinates as a tridentate O,N,O donor while the sulfur side-arm donor remains intact. The solid-state structure of 2a was investigated by X-ray crystallography.
Dioxomolybdenum(VI) and oxotungsten(VI) complexes with a new amine bisphenol ligand (H(2)L) are reported. The ligand which carries a neutral nitrogen atom, two phenolic oxygen atoms and a thiophene side-arm was synthesized by a simple one-pot Mannich reaction. Further reaction with [MoO(2)(acac)(2)] yielded a monomeric molybdenum complex [MoO(2)(L)(MeOH)] (2a) or a dimeric complex [Mo(2)O(2)(mu-O)(2)(L)(2)] (2b), depending on the reaction conditions. The reaction with a tungsten trisglycolate [W(eg)(3)] led to the formation of a monomeric compound [WO(eg)(L)] (3). In these complexes, the potentially tetradentate amine bisphenolate dianion coordinates as a tridentate O,N,O donor while the sulfur side-arm donor remains intact. The solid-state structure of 2a was investigated by X-ray crystallography.
Turun yliopiston Tutkimustietojärjestelmän portaali