Exploring the Lewis basicity of the metalloligand [Pt₂(μ-Se)₂(PPh₃)₄] on metal substrates by electrospray mass spectrometry. Synthesis, characterization and structural studies of new platinum selenido phosphine complexes containing the {Pt₂Se₂} core

Electrospray Mass Spectrometry (ESMS) has been used as a tool to probe the reactivity of the metalloligand [Pt₂(μ-Se)₂(PPh₃)₄] with metal substrates, which lead to the formation of charged coordination complexes via loss of halides or other labile ligands. Among the numerous metal substrates used in the displacement reactions are Au(anpy)Cl₂ (anpy = cyclometallated 2-anilinopyridyl), HgPhCl and Pb(NO₃)₂. Acid titration on the Lewis basic metalloligand leads to the identification and isolation of the doubly-protonated species, [Pt₂(μ-SeH)₂(PPh₃)₄]²⁺, whose sulfide analogue cannot be isolated. A three-step strategy is employed in the use of ESMS as a probe: (i) preliminary screening of the metalloligand with an array of acidic main group and transition group metal compounds, (ii) identification of potentially stable and isolable products formed in situ based on ion distribution and simulated isotope patterns and (iii) promising reactions are repeated on a laboratory scale, and target products are isolated and characterized. X-Ray diffraction studies have been performed on single crystals of [Pt₂(μ-SeH)₂(PPh₃)₄][ClO₄]₂, [Pt₂(μ₃-Se)₂(PPh₃)₄(CdCl₂)] and {Pt₂(μ₃-Se)₂(PPh₃)₄[Pb(NO₃)]}{NO₃}. These results suggested that in general a parallel chemistry can be developed on the intermetallic selenides as on the sulfides. However, there are chemical and structural differences which are highlighted in this paper

Mass spectrometry-directed synthesis of early–late sulfide-bridged heterobimetallic complexes from the metalloligand [Pt₂(PPh₃)₄(μ-S)₂] and oxo compounds of vanadium(V), molybdenum(VI) and uranium(VI)

The metalloligand [Pt₂(PPh₃)₄(μ-S)₂] has been found to react with the transition metal oxo compounds, ammonium metavanadate, sodium molybdate, and the actinide complex uranyl nitrate to give sulfide-bridged heterobimetallic complexes [Pt₂(PPh₃)₄(μ₃-S)₂VO(OMe)₂]⁺, [Pt₂(PPh₃)₄(μ₃-S)₂MoO₂(OMe)]⁺, and [Pt₂(PPh₃)₄(μ₃-S)₂UO₂( ₂-NO₃)₂], respectively. Electrospray mass spectrometry (ESMS) was used to probe the reactivity of [Pt₂(PPh₃)₄(μ-S)₂] and thus identify likely targets for isolation and characterization. ESMS has also been used to investigate fragmentation pathways of the new species. No bimetallic species were detected with hydrated La(NO₃)₃or Th(NO₃)₄, or with the lanthanide shift reagent Eu(fod)₃ (fod = 6,6,7,7,8,8,8-heptafluoro-2,2-dimethyl-3,5-octanedionate). X-Ray crystal structure determinations have been carried out on [Pt₂(PPh₃)₄(μ₃-S)₂VO(OMe)₂]⁺, 2, (as its hexafluorophosphate salt) and [Pt₂(PPh₃)₄(μ₃-S)₂UO₂( ₂-NO₃)₂], 4. The vanadium atom of 2 has a distorted square pyramidal geometry, while the uranium in 4 has the expected linear dioxo coordination geometry, with two bidentate nitrates and a bidentate {Pt₂S₂} moiety

A rapid screening, “combinatorial-type” survey of the metalloligand chemistry of Pt₂(PPh₃)₄(μ-S)₂ using electrospray mass spectrometry

Electrospray mass spectrometry is a rapid and powerful technique for a combinatorial-like survey of the chemistry of the metalloligand Pt₂(PPh₃)₄(μ-S)₂, leading to the successful isolation and crystallographic characterisation of the novel protonated species Pt₂(PPh₃)₄(μ-S)(μ-SH) together with a range of metallated derivatives

Catecholase-like activity in 2D MOFs: Oxidation of 3,5-DTBC by two Cu(II) 2D MOFs of reduced Schiff base ligands

10.1016/j.ica.2021.120502INORGANICA CHIMICA ACTA52

Control of interpenetration and structural transformations in the interpenetrated MOFs

10.1016/j.ccr.2021.213789COORDINATION CHEMISTRY REVIEWS43

Regulating thermosalient behaviour in three polymorphs

10.1107/S2052252517005577IUCrJ4202-20

Isomerization of cyclobutane ligands in the solid state and solution

10.1016/j.jics.2022.100630JOURNAL OF THE INDIAN CHEMICAL SOCIETY99

Photoreactive Crystals Exhibiting [2+2] Photocycloaddition Reaction and Dynamic Effects

10.1021/acs.accounts.2c00107ACCOUNTS OF CHEMICAL RESEARCH55101445-145

Dynamic effects in crystalline coordination polymers

10.1039/d1ce00441gCRYSTENGCOMM23345738-575

Mechanical Bending and Modulation of Photoactuation Properties in a One-Dimensional Pb(II) Coordination Polymer

10.1021/acs.chemmater.1c01124CHEMISTRY OF MATERIALS33124621-462