about
Samb V ca: A Web Application for the Calculation of the Buried Volume of N-Heterocyclic Carbene LigandsStructural Preferences in Phosphanylthiolato Platinum(II) ComplexesAtropisomeric discrimination in new Ru(II) complexes containing the C(2)-symmetric didentate chiral phenyl-1,2-bisoxazolinic ligand.Fast O2 binding at dicopper complexes containing Schiff-base dinucleating ligands.Identification and characterization of a new family of catalytically highly active imidazolin-2-ylidenes.[{Au(IPr)}2(μ-OH)]X complexes: synthetic, structural and catalytic studies.Pesticides Curbing Soil Fertility: Effect of Complexation of Free Metal Ions.Facile C-H bond cleavage via a proton-coupled electron transfer involving a C-H...Cu(II) interaction.Mechanism of the Transmetalation of Organosilanes to Gold.On the Reaction Mechanism of the Rhodium-Catalyzed Arylation of Fullerene (C60) with Organoboron Compounds in the Presence of WaterComputational methods to predict the reactivity of nanoparticles through structure-property relationships.Modeling the structure-property relationships of nanoneedles: A journey toward nanomedicine.Complete σ* intramolecular aromatic hydroxylation mechanism through O2 activation by a Schiff base macrocyclic dicopper(I) complex.The Right Computational Recipe for Olefin Metathesis with Ru-Based Catalysts: The Whole Mechanism of Ring-Closing Olefin Metathesis.Versatile deprotonated NHC: C,N-bridged dinuclear iridium and rhodium complexesSimple activation by acid of latent Ru-NHC-based metathesis initiators bearing 8-quinolinolate co-ligandsStructural Preferences in Phosphanylthiolato Platinum(II) Complexes.A comprehensive study of olefin metathesis catalyzed by Ru-based catalystsO2 chemistry of dicopper complexes with alkyltriamine ligands. Comparing synergistic effects on O2 binding.Comparing the enantioselective power of steric and electrostatic effects in transition-metal-catalyzed asymmetric synthesis.C2-symmetric chiral disulfoxide ligands in rhodium-catalyzed 1,4-addition: from ligand synthesis to the enantioselection pathway.Mechanistic insights into the cis-trans isomerization of ruthenium complexes relevant to catalysis of olefin metathesis.A versatile gold synthon for acetylene C-H bond activation.Flexibility of N-heterocyclic carbene ligands in ruthenium complexes relevant to olefin metathesis and their impact in the first coordination sphere of the metal.Comparing families of olefin polymerization precatalysts using the percentage of buried volume.The activation mechanism of Ru-indenylidene complexes in olefin metathesis.Ruthenium complexes with chiral bis-pinene ligands: an array of subtle structural diversity.Energetics of the ruthenium-halide bond in olefin metathesis (pre)catalysts.Exploring new generations of ruthenium olefin metathesis catalysts: the reactivity of a bis-ylidene ruthenium complex by DFT.Regioselective intramolecular Pauson-Khand reactions of C60: an electrochemical study and theoretical underpinning.Exploring the reactivity of Ru-based metathesis catalysts with a pi-acid ligand trans to the Ru-ylidene bond.Complete mechanism of sigma* intramolecular aromatic hydroxylation through O2 activation by a macrocyclic dicopper(I) complex.Cover Picture: Structural Preferences in Phosphanylthiolato Platinum(II) Complexes (ChemistryOpen 1/2016).New ruthenium(II) complexes with enantiomerically pure bis- and tris(pinene)-fused tridentate ligands. Synthesis, characterization and stereoisomeric analysis.Synthesis and Isomeric Analysis of Ru(II) Complexes Bearing Pentadentate Scaffolds.Moving from Classical Ru-NHC to Neutral or Charged Rh-NHC Based Catalysts in Olefin Metathesis.On the Mechanism of the Digold(I)-Hydroxide-Catalysed Hydrophenoxylation of Alkynes.Cooperative Effect of Monopodal Silica-Supported Niobium Complex Pairs Enhancing Catalytic Cyclic Carbonate Production.Exploring the mechanism of Grignard metathesis polymerization of 3-alkylthiophenes.Insights into the decomposition of olefin metathesis precatalysts.
P50
Q27144118-7ED1B8C8-57B5-48E6-9BEA-3E63AE221E3FQ28830450-B76AC214-B5D2-4BA8-BD14-DB856072C8CDQ31029836-F2F67AEF-0538-40BE-AD1A-4EE1F992FCCDQ31112519-20ED6F6C-B110-4FC4-89DC-61B67A08296BQ31153901-0A107A58-5C22-4D26-91A3-565DBBC18C3BQ33796023-805179EC-C0AC-47D7-A99F-D8F958231336Q33867112-6A325DA0-7B10-4A3D-A21C-D1AE437A98D5Q34120995-0F4DC22E-B2C7-43C6-B84A-FF62D9653672Q37000771-71D1060C-991F-454B-AE89-0E86990D5DD9Q37000793-F4FC1350-BD5F-4D03-BE36-A749AF040C45Q37702249-5605F270-302A-4D29-8AB7-A6CDDA24E1ADQ38572410-36DCEED4-8CF2-42EC-9C3C-A57C9F9FBB36Q39911037-10292CDA-BC19-463B-AD48-78A1C562E95FQ40297438-387590F9-AC2C-407D-A31C-F3472FC4C9BCQ41906295-E55AA4B2-AF8B-4D30-A184-4BB7A956CD34Q41918694-F55163C0-12A9-4647-9F0B-D226C2E0E41AQ42072586-180ACF7B-3463-490D-9881-0732522C86CCQ42131335-0FB5A16F-65A9-4CFE-9B1F-AEDEF319EEACQ42419866-3DBA1CF8-57B5-4B7D-B59A-CB3C5886EA08Q42808138-65465D8D-F901-45DA-A206-480EADC2A27DQ42815774-4FF321BA-D377-41D7-8A37-0A651B55490EQ42835859-1B70918D-F31F-413B-BFE6-DF70D1CA1841Q42869968-5855C08D-DED7-41A1-A50A-4B33707E4F06Q43141880-61234F3C-8052-4955-BFF7-9EF28DA64127Q43262005-29502D80-F5DA-4E12-85E8-D0BE73936E9FQ43536983-D63F8A37-59EC-4ADC-9CC7-B1027485F73BQ44146788-702DAC3B-9643-4356-BE44-C77E030A46A0Q44232819-3927C16C-4F0E-4B8D-A36B-3942129AF79CQ44434165-91070DC3-A20E-47CE-B483-5CB77256B550Q45281676-08AA3D99-EFFA-4FEB-8BBA-A6C33E3FEC91Q45978503-7F664E7E-572C-4D73-86B5-4F082CAEEDD8Q46214957-931C1F18-3360-4B7E-9021-5D50D03F19C3Q46410233-8F1B1826-7497-46E5-A596-7046EFD45AB3Q46435587-EDAE4704-C6B3-4F64-A955-CBF4145E39BDQ46492130-D5D82A49-2B0B-4CE2-85E1-CE11740CE23DQ46601225-307CB6E5-49A1-47DE-9998-D693184A562DQ46624576-C0FA9D22-EFCF-4502-87E2-59162A412F53Q46731872-AF7C1F1B-0EBD-4593-93C9-46306E5B8CB1Q46844596-793D5C27-8442-4F28-8135-843DFC8D9B93Q46885018-CE3FF2ED-AE9E-41DE-9F44-1382447065F3
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
ricercatore
@it
հետազոտող
@hy
name
Albert Poater
@ast
Albert Poater
@en
Albert Poater
@es
Albert Poater
@nl
type
label
Albert Poater
@ast
Albert Poater
@en
Albert Poater
@es
Albert Poater
@nl
prefLabel
Albert Poater
@ast
Albert Poater
@en
Albert Poater
@es
Albert Poater
@nl
P214
P1053
D-6586-2013
P106
P1153
8533443400
P21
P214
P2798
P31
P3829
P496
0000-0002-8997-2599
P735
P7859
viaf-311585866