Search results for "Ylide"
showing 10 items of 1084 documents
Atom transfer radical polymerization with different halides (F, Cl, Br, and I): Is the process "living" in the presence of fluorinated initiators?
2016
Atom transfer radical polymerization (ATRP) is often used for grafting from fluorinated polymers. Nevertheless, the possibility to initiate an ATRP from a C-F functionality and the activity of the catalysts in the presence of fluoride anions are essentially unexplored. Therefore, we investigated the thermodynamics and kinetics of C-F bond activation by ATRP catalysts and compared it with other halide systems. The ATRP equilibrium constant was estimated to be small for the reaction between [CuITPMA]+ and benzyl fluoride (TPMA = tris(2-pyridylmethyl)- amine). However, [CuITPMA] + could react with the more active initiator diethyl fluoromalonate (DEFM). With DEFM as initiator and CuIBr/TPMA as…
Influence of high power ultrasound on physical-chemical properties of polypropylene films aimed for food packaging: barrier and contact angle features
2017
Investigation was focused on the impact of high power ultrasound (HPUS), also called thermosonication, on the oxygen permeation properties (permeability, solubility and diffusion coefficients) of barrier films aimed for food packaging. For this purpose, biaxially oriented polypropylene (BOPP) coated with acrylic/polyvinylidene chloride (BOPPAcPVDC) and biaxially oriented coextruded polypropylene (BOPPcoex) were used. The physical–chemical profile of the samples was determined using goniometry. There is a significant impact only of extreme HPUS conditions (the longest time and the highest amplitude) on the permeability, solubility and diffusion coefficients of oxygen through the BOPP films. …
A DFT study of the mechanism and selectivities of the [3 + 2] cycloaddition reaction between 3-(benzylideneamino)oxindole and trans -β-nitrostyrene
2016
The mechanism and regioselectivities and stereoselectivities of the [3 + 2] cycloaddition (32CA) reaction of 3-(benzylideneamino) oxindole (AY) and trans-β-nitrostyrene have been studied using both B3LYP and ωB97XD density functional theory methods together with the standard 6-31G(d) basis set. Four reactive pathways associated with the ortho and meta regioselective channels and endo and exo stereoselective approaches modes have been explored and characterized. While the B3LYP functional fails to predict the experimental regioselectivity, the ωB97XD one succeeds to predict the experimentally observed meta regioselectivity favoring the formation of meta/endo cycloadduct as the major isomer. …
CCDC 854063: Experimental Crystal Structure Determination
2012
Related Article: A.Molina-Ontoria, R.Garcia, A.Gouloumis, F.Giacalone, M.R.Torres, N.Martin|2012|Eur.J.Org.Chem.|2012|3581|doi:10.1002/ejoc.201200115
CCDC 1439186: Experimental Crystal Structure Determination
2016
Related Article: Toni Mäkelä, Miia-Elina Minkkinen, and Kari Rissanen|2016|Inorg.Chem.|55|1339|doi:10.1021/acs.inorgchem.5b02780
CCDC 224283: Experimental Crystal Structure Determination
2004
Related Article: J.Vicente, M.-T.Chicote, M.D.Abrisqueta, M.M.Alvarez-Falcon, M.C.R.de Arellano, P.G.Jones|2003|Organometallics|22|4327|doi:10.1021/om030372r
CCDC 194090: Experimental Crystal Structure Determination
2003
Related Article: M.Poyatos, E.Mas-Marza, J.A.Mata, M.Sanau, E.Peris|2003|Eur.J.Inorg.Chem.||1215|doi:10.1002/ejic.200390157
CCDC 619714: Experimental Crystal Structure Determination
2006
Related Article: M.Cametti, M.Nissinen, A.D.Cort, K.Rissanen, L.Mandolini|2006|Inorg.Chem.|45|6099|doi:10.1021/ic060251u
CCDC 977406: Experimental Crystal Structure Determination
2016
Related Article: Christoph Deckert, Denis Bittner, Luca M. Carrella, Dieter Schollmeyer and Eva Rentschler|2016|Eur.J.Inorg.Chem.||1738|doi:10.1002/ejic.201501400
CCDC 1534659: Experimental Crystal Structure Determination
2017
Related Article: Karolina Zdyb, Maxym O. Plutenko, Rostislav D. Lampeka, Matti Haukka, Malgorzata Ostrowska, Igor O. Fritsky, Elzbieta Gumienna-Kontecka|2017|Polyhedron|137|60|doi:10.1016/j.poly.2017.07.009