More user-friendly phosphines? Molecular structure of methylphosphine and its adduct with borane, studied by gas-phase electron diffraction and quantum chemical calculations-Reference-Cited by-同舟云学术

More user-friendly phosphines? Molecular structure of methylphosphine and its adduct with borane, studied by gas-phase electron diffraction and quantum chemical calculations

Published:2008 Issue:37 Volume: Page:5041
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Noble-Eddy Robert,Masters (née Hinchley) Sarah L.,Rankin David W. H.,Wann Derek A.,Khater Brahim,Guillemin Jean-Claude

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2008/DT/B804780D

Reference47 articles.

1. Towards “user-friendly” heavier primary pnictanes: Recent developments in the chemistry of primary phosphines, arsines and stibines

2. Bildung und Eigenschaften von Acylphosphanen. VI. Synthese von Alkyl- und Arylbis (trimethylsilyl)- sowie Alkyl und Aryltrimethylsilyphosphanen

3. PH bond activation of primary phosphine-boranes: Access to α-hydroxy and α,α′-dihydroxyphosphine-borane adducts by uncatalyzed hydrophosphination of carbonyl derivatives

4. Transition Metal-Catalyzed Formation of Phosphorus−Boron Bonds: A New Route to Phosphinoborane Rings, Chains, and Macromolecules

5. Structure Analysis Restrained by ab Initio Calculations: The Molecular Structure of 2,5-Dichloropyrimidine in Gaseous and Crystalline Phases

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