about
New perspectives for "non-classical" molecules: heavy [1.1.1]propellanes of group 14.Reactivity in the periphery of functionalised multiple bonds of heavier group 14 elements.On the Ambiphilic Reactivity of Geometrically Constrained Phosphorus(III) and Arsenic(III) Compounds: Insights into Their Interaction with Ionic Substrates.Stable singlet carbenes as mimics for transition metal centers.E-H Bond Activation of Ammonia and Water by a Geometrically Constrained Phosphorus(III) Compound.Activation of gaseous PH3 with low coordinate diaryltetrylene compounds.A nitrogen-base catalyzed generation of organotin(ii) hydride from an organotin trihydride under reductive dihydrogen elimination.On the Redox Reactivity of a Geometrically Constrained Phosphorus(III) Compound.Reactions of heavier main-group compounds with hydrogen, ammonia, ethylene and related small molecules.N,P-Heterocyclic Germylene/B(C6 F5 )3 Adducts: A Lewis Pair with Multi-reactive Sites.Reductive Elimination of Hydrogen from Bis(trimethylsilyl)methyltin Trihydride and Mesityltin Trihydride.Ligand coordination modulates reductive elimination from aluminium(iii).Activation of Dihydrogen by Masked Doubly Bonded Aluminum Species.Base-Stabilized Phosphinidene Boranes by Silylium-Ion Abstraction.Addition of ethylene or hydrogen to a main-group metal cluster under mild conditions.Less is more: three-coordinate c,n-chelated distannynes and digermynes.Access to Base Adducts of Low-Valent Organotin-Hydride Compounds by Controlled, Stepwise Hydrogen Abstraction from a Tetravalent Organotin Trihydride.Dimeric platinum-stannylene complexes by twofold ligand transfer from an NHC adduct to an organotin(II) hydride.Uncatalyzed Hydrogenation of First-Row Main Group Multiple Bonds.Formation of a unique 'unsupported' hydridic stannate(II).A P4 Chain and Cage from Silylene-Activated White PhosphorusA P4 Chain and Cage from Silylene-Activated White PhosphorusImpact of a rigid backbone on the structure of an agostically-stabilised dialkylstannylene: isolation of an unusual bridged stannyl–stannylene
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Addition of H2 to distannynes under ambient conditions.
@en
Addition of H2 to distannynes under ambient conditions.
@nl
type
label
Addition of H2 to distannynes under ambient conditions.
@en
Addition of H2 to distannynes under ambient conditions.
@nl
prefLabel
Addition of H2 to distannynes under ambient conditions.
@en
Addition of H2 to distannynes under ambient conditions.
@nl
P2093
P356
P1476
Addition of H2 to distannynes under ambient conditions
@en
P2093
Bobby D Ellis
Eric Rivard
Marcin Brynda
Philip P Power
P304
P356
10.1039/B813442A
P407
P577
2008-10-17T00:00:00Z