volume 355 pages 150-172

POP-type ligands: Variable coordination and hemilabile behaviour

Publication typeJournal Article
Publication date2018-01-01
scimago Q1
wos Q1
SJR4.638
CiteScore38.2
Impact factor23.5
ISSN00108545, 18733840
Materials Chemistry
Inorganic Chemistry
Physical and Theoretical Chemistry
Abstract
Hemilabile ligands – ligands containing two or more potential donors to a metal centre, of which one or more can dissociate – have the ability to provide a transition metal complex with open coordination sites at which reactivity can occur, or stabilise low coordinate intermediates along reaction pathways. POP-type ligands and in particular POP, Xantphos, DBFphos and DPEphos-based ligands contain three possible binding sites: two phosphines and an ether linker, thus have the potential to show κ1-, κ2- or κ3-binding modes. This review summarises the examples where POP-type ligands display hemilabile, or closely related variable coordination, characteristics in either synthesis or catalysis.
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Adams G. M., Weller A. E. POP-type ligands: Variable coordination and hemilabile behaviour // Coordination Chemistry Reviews. 2018. Vol. 355. pp. 150-172.
GOST all authors (up to 50) Copy
Adams G. M., Weller A. E. POP-type ligands: Variable coordination and hemilabile behaviour // Coordination Chemistry Reviews. 2018. Vol. 355. pp. 150-172.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.ccr.2017.08.004
UR - https://doi.org/10.1016/j.ccr.2017.08.004
TI - POP-type ligands: Variable coordination and hemilabile behaviour
T2 - Coordination Chemistry Reviews
AU - Adams, Gemma M
AU - Weller, Andrew E.
PY - 2018
DA - 2018/01/01
PB - Elsevier
SP - 150-172
VL - 355
SN - 0010-8545
SN - 1873-3840
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2018_Adams,
author = {Gemma M Adams and Andrew E. Weller},
title = {POP-type ligands: Variable coordination and hemilabile behaviour},
journal = {Coordination Chemistry Reviews},
year = {2018},
volume = {355},
publisher = {Elsevier},
month = {jan},
url = {https://doi.org/10.1016/j.ccr.2017.08.004},
pages = {150--172},
doi = {10.1016/j.ccr.2017.08.004}
}