138-87-4Relevant articles and documents
Organometallic Mo complex anchored to magnetic iron oxide nanoparticles as highly recyclable epoxidation catalyst Dedicated to Prof. Maria José Calhorda on the occasion of her 65th birthday
Fernandes, Cristina I.,Carvalho, Maria Deus,Ferreira, Liliana P.,Nunes, Carla D.,Vaz, Pedro D.
, p. 2 - 10 (2014)
The organometallic fragment [MoI2(CO)3] was coordinated to magnetic iron oxide nanoparticles of different sizes (average size of 11 and 30 nm) which have been previously coated with a silica shell and grafted with a pyridine derivative ligand. The Mo loading was found to be approximately 0.37 wt-% Mo and 0.57 wt-% Mo, corresponding to 0.150 mmol Mo g-1 and 0.230 mmolMo g-1 for materials MNP30-Si-inic-Mo and MNP11-Si-inic-Mo, respectively. Preparation of these organometallic decorated magnetic nanoparticles was further confirmed by evidence obtained from extensive characterization by powder XRD, SEM/TEM analysis, as well as from data of 57Fe M?ssbauer and FTIR spectroscopy. Olefin epoxidation of a variety of substrates promoted by these organometallic nano-hybrid materials using tbhp as oxidant, was performed with very good results. The catalytic studies show that the catalysts yield selectively the desired epoxides of a series of olefins. In addition, these catalysts are found to work under a wide temperature range and over several catalytic cycles without notorious performance loss in most cases.
Synthesis, Characterization, Magnetic and Catalytic Properties of a Ladder-Shaped MnII Coordination Polymer
Lymperopoulou, Smaragda,Papastergiou, Maria,Louloudi, Maria,Raptopoulou, Catherine P.,Psycharis, Vassilis,Milios, Constantinos J.,Plakatouras, John C.
, p. 3638 - 3644 (2015/04/27)
[Mn(LH)(H2O)]n {1, where LH2- is the dianion of N-(4-carboxybenzyl)iminodiacetic acid} has been synthesized and its crystal structure has been determined. The crystal of 1 is built from 1D polymeric ladder-shaped chains that extend to a 3D supramolecular architecture through H-bonds. The compound was characterized with spectroscopic and physicochemical techniques. Variable-temperature magnetic data suggest that there are weak antiferromagnetic interactions. Compound 1 has been evaluated as a heterogeneous oxidation catalyst. It catalyzes alkene epoxidation selectively in relatively high yields.
Lithium-potassium superbases as key reagents for the base-catalysed isomerisation of some terpenoids
Deagostino,Tivola,Prandi,Venturello
, p. 2856 - 2860 (2007/10/03)
Some representative monoterpenes have been isomerised under the influence of Schlosser's lithium-potassium mixed superbases, promoting β-elimination reactions. The results are compared with those obtained with butyllithium and LDA. Different selectivities and different reaction yields are achieved as a function of the base employed. These results confirm the particular reactivity of bimetallic reagents. In this paper it is proposed that the observed selectivities might depend on the conformational features of the substrate, on the strength of the organometallic reagent, as well as on steric requirements of the elimination reaction.
