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@article{Phanopoulos:2015:10.1016/j.ccr.2015.04.001,
author = {Phanopoulos, A and Miller, PW and Long, NJ},
doi = {10.1016/j.ccr.2015.04.001},
journal = {Coordination Chemistry Reviews},
pages = {39--60},
title = {Beyond Triphos - New hinges for a classical chelating ligand},
url = {http://dx.doi.org/10.1016/j.ccr.2015.04.001},
volume = {299},
year = {2015}
}

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TY  - JOUR
AB  - Branched triphosphine ligands have been less widely studied than mono- and bi-dentate analogues. The most studied ligand of this type is TriphosPh (CH3C(CH2PPh2)3). Substitution of the apical Csingle bondCH3 moiety with boron, silicon, tin, nitrogen or phosphorus fragments has generated a new family of ligands, in some cases displaying varying coordination chemistry and reactivity to the parent carbon-based system. This review includes the synthetic strategies implemented to afford these ligands, as well as derivatives by way of varying the phosphine substituents. Although not exhaustive, relevant types of reported complexes featuring these ligands are discussed, as well as their reactivity and catalytic applications. Through critical analysis, common themes and chemical trends across this family of apical heteroatomic, branched triphosphines can be identified, leading to improvements in current chemical applications, as well as new areas that remain underdeveloped.
AU  - Phanopoulos,A
AU  - Miller,PW
AU  - Long,NJ
DO  - 10.1016/j.ccr.2015.04.001
EP  - 60
PY  - 2015///
SN  - 1873-3840
SP  - 39
TI  - Beyond Triphos - New hinges for a classical chelating ligand
T2  - Coordination Chemistry Reviews
UR  - http://dx.doi.org/10.1016/j.ccr.2015.04.001
UR  - http://hdl.handle.net/10044/1/25452
VL  - 299
ER  -

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