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Yusuf Hamied Department of Chemistry

 

University Assistant Professor

Research interests

The Webster group focuses on catalysis with first row transition metals, with a focus on iron catalyst design for the synthesis of bonds between main-group elements. We are interested in trying to understand mechanism and in order to do so we use a varity of in situ and in-line techniques.

 

Watch Dr Webster discuss her research

Publications

Room temperature iron catalyzed transfer hydrogenation usingn-butanol and poly(methylhydrosiloxane)
TG Linford-Wood, NT Coles, RL Webster
– Green Chemistry
(2021)
23,
2703
Correction: Room temperature iron catalyzed transfer hydrogenation using n -butanol and poly(methylhydrosiloxane)
TG Linford-Wood, NT Coles, RL Webster
– Green Chemistry
(2021)
23,
3750
Regioselective Alkyne Cyclotrimerization with an In Situ-Generated [Fe(II)H(salen)]·Bpin Catalyst
CB Provis-Evans, S Lau, V Krewald, RL Webster
– ACS Catalysis
(2020)
10,
10157
Highly Sensitive Real-Time Isotopic Quantification of Water by ATR-FTIR.
CB Provis-Evans, EHE Farrar, MN Grayson, RL Webster, AK Hill
– Analytical chemistry
(2020)
92,
7500
Seeking Heteroatom-Rich Compounds: Synthetic and Mechanistic Studies into Iron Catalyzed Dehydrocoupling of Silanes
D Gasperini, AK King, NT Coles, MF Mahon, RL Webster
– ACS Catalysis
(2020)
10,
6102
Hydrophosphination using [GeCl{N(SiMe3)2}3] as a pre-catalyst
AN Barrett, HJ Sanderson, MF Mahon, RL Webster
– Chemical communications (Cambridge, England)
(2020)
56,
13623
Room Temperature Iron-Catalyzed Transfer Hydrogenation and Regioselective Deuteration of Carbon-Carbon Double Bonds.
M Espinal-Viguri, SE Neale, NT Coles, SA Macgregor, RL Webster
– J Am Chem Soc
(2018)
141,
572
Room Temperature Ni(II) Catalyzed Hydrophosphination and Cyclotrimerization of Alkynes
RL Webster
– Inorganics
(2018)
6,
120
Rapid Metal-Free Formation of Free Phosphines from Phosphine Oxides
CB Provis-Evans, EAC Emanuelsson, RL Webster
– Advanced Synthesis & Catalysis
(2018)
360,
3999
1,1-Diphosphines and divinylphosphines via base catalyzed hydrophosphination.
NT Coles, MF Mahon, RL Webster
– Chemical communications (Cambridge, England)
(2018)
54,
10443
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Research Group

Research Interest Group

Telephone number

01223 336405

Email address

rw740@cam.ac.uk