Peter Maitlis

Peter Michael Maitlis, FRS (15 January 1933 – 18 May 2022) was a British organometallic chemist.

Maitlis was born on 15 January 1933, and educated at Hendon School (then Hendon County School) in north London 1944–50.

He was awarded a Bachelor's degree in Science from the University of Birmingham, and a PhD (1956, studying under Professor Michael J. S. Dewar, who helped to develop the Dewar–Chatt–Duncanson model for bonding in organometallic compounds) and a DSc (1970) from the University of London.

After completing his doctorate, Maitlis worked as an Assistant Lecturer at the University of London.

He undertook postdoctoral study at Cornell University as a Fulbright Fellow (1960–1961) and then as a research fellow at Harvard University (1961–1962) under F. G. A. Stone.

While working and teaching at McMaster University in Hamilton, Ontario (1962–1972), he rose from Assistant Professor to a full Professorship.

In 1971, he published two volumes on the organic chemistry of palladium which were "widely recognised as the most authoritative account of the organo-complexes of this metal".

Returning to the United Kingdom in 1972, Maitlis was a professor of chemistry at the University of Sheffield for 30 years until his appointment as an emeritus professor in 2002.

They have been a research interest of Maitlis' group since the mid-1980s, and in fact Maitlis jointly directed the early investigations of these systems in the UK and actually coined the term metallomesogen.

Maitlis was Jewish.

He was the father of the journalist and newsreader Emily Maitlis.

He died on 18 May 2022, at the age of 89.

The following list shows the top 10 most cited journal articles by Maitlis according to Web of Science data.

The number of citations indicated is current as at 27 May 2022:

Maitlis was elected a Fellow of the Royal Society in 1984.

The citation highlights his work on the platinum group metals palladium, rhodium and iridium.

The hexafluorophosphate ion is generally considered inert and hence a suitable counterion in organometallic synthesis.

However, Maitlis' work has demonstrated a solvolysis reaction of the hexafluorophosphate ion.

The tris(solvent) rhodium complex [(η5-C5Me5)Rh(Me2CO)3](PF6)2 undergoes solvolysis when heated in acetone, forming a difluorophosphate-bridged complex [(η5-C5Me5)Rh(μ-OPF2O)3Rh(η5-C5Me5)]PF6.

Hexamethyl Dewar benzene (C6Me6) undergoes an unusual rearrangement reaction with hydrohalic acids to form a pentamethylcyclopentadiene derivative, and consequently can be used as a starting material for synthesising some pentamethylcyclopentadienyl organometallic compounds.

Maitlis and colleagues demonstrated this synthesis and its applicability to the iridium analogue, [(η5-C5Me5)IrCl2]2.

His group also demonstrated a more convenient synthesis for the bright orange, air-stable diamagnetic iridium reagent using pentamethylcyclopentadiene.

Isocyanides can serve as ligands in co-ordination chemistry as a result of the lone electron pair on carbon, and are especially useful with metals in the 0, +1, and +2 oxidation states.

In particular, Maitlis has demonstrated that tert-butyl isocyanide can stabilise metals in unusual oxidation states, such as palladium(I) in the complex [(t-BuNC)2Pd(μ-Cl)]2.

Metallomesogens are "metal complexes of organic ligands which exhibit liquid crystalline (mesomorphic) character [and thus they] combine the variety and range of metal-based coordination chemistry with the extraordinary physical properties exhibited by liquid crystals."