13122-41-3Relevant articles and documents
Electronic and Ion-Pairing Effects of a Methyl Group on a Diphenylmethyl Anion Determined by Restricted Aryl Rotation
Bank, Shelton,Marcantonio, Richard P.,Bushweller, C. H.
, p. 5091 - 5093 (1984)
The compound lithium has been prepared and studied by 1H DNMR.A complete line shape analysis of the spectrum allows unambiguous phenyl ring assignment to the differential aryl barriers to rotation.Solvent v
Parallel NMR based on solution magnetic-susceptibility differences. Application to isotopic effects on self-diffusion
Fries, Pascal H.,Imbert, Daniel
experimental part, p. 2048 - 2054 (2011/07/30)
Different susceptibility NMR line shifts can be induced in distinct liquid solutions by dissolving different concentrations of complexes of paramagnetic lanthanide Ln3+ ions. We show how these solutions, put in capillaries, can be simultaneousl
The conformational distribution in diphenylmethane determined by nuclear magnetic resonance spectroscopy of a sample dissolved in a nematic liquid crystalline solvent
Celebre,De Luca,Emsley,Foord,Longeri,Lucchesini,Pileio
, p. 6417 - 6426 (2007/10/03)
The application of the probabilistic approach, coupled with the AP model for the conformational dependence of the interaction with liquid crystal molecules, gives a distribution PLC(τ1, τ2) which is similar to that found b
Is the collosion induced loss of ethene from the (M - H+)- ion of butyrophenone a γ-hydrogen rearrangement?
Stringer, Michael B.,Underwood, Dennis J.,Bowie, John H.,Holmes, John L.,Mommers, Alexander A.,Szulejko, Jan E.
, p. 764 - 768 (2007/10/02)
The (M - H+)- ion of butyrophenone undergoes the following reactions on collisional activation: losses of CH3., CH4, (C,H5.), C2H4, C3H7., (CO + CH4), together with formation of C6H5- and C
