A family of zinc phosphate complexes supported by nitrogen donor-base ligands have been synthesized, and their molecular structures were identified in both the solid (X-ray crystallography) and solution state (DOSY NMR spectroscopy). [Zn{OP(OPh)}] (), formed from the reaction of Zn[N(SiMe)] with HO(O)P(OPh) coordinates to donor-base ligands, , pyridine (Py), 4-methylpyridine (4-MePy), 2,2-bipyridine (bipy), tetramethylethylenediamine (TMEDA), pentamethyldiethylenetriamine (PMDETA), and 1,3,5-trimethyl-1,3,5-triazacyclohexane (Me-TAC), to produce polymeric 1D structures, [(Py)Zn{OP(OPh)}] () and [(4-MePy)Zn{OP(OPh)}] (), the bimetalic systems, [(Bipy)Zn{OP(OPh)}] (), [(TMEDA)Zn{OP(OPh)}] (), and [(Me-TAC)Zn{OP(OPh)}] (), as well as a mono-nuclear zinc bis-diphenylphosphate complex, [(PMDETA)Zn{OP(OPh)}] (). H NMR DOSY has been used to calculate averaged molecular weights of the species. Studies are consistent with the disassembly of polymeric into the bimetallic species [(Me-Py)·Zn{OP(OPh)}], where the Me-Py ligand is in rapid exchange with free Me-Py in solution. Further H DOSY NMR studies of and reveal that dissolution of the complex results in a monomer dimer equilibrium, , [(Bipy)Zn{OP(OPh)}] ⇆ 2[(Bipy)Zn{OP(OPh)}] and [(TMEDA)Zn{OP(OPh)}] ⇆ 2[(TMEDA)Zn{OP(OPh)}], respectively, in which the equilibria lie toward formation of the monomer. As part of our studies, variable temperature H DOSY experiments (223 to 313 K) were performed upon in -tol, which allowed us to approximate the enthalpy [Δ = -43.2 kJ mol (±3.79)], entropy [Δ = 109 J mol K (±13.9)], and approximate Gibbs free energy [Δ = 75.6 kJ mol (±5.62) at 293 K)] of monomer-dimer equilibria. While complex is shown to maintain its monomeric solid-state structure, H DOSY experiments of at 298 K reveal two separate normalized diffusion coefficients consistent with the presence of the bimetallic species [(TAC)Zn{OP(OPh)}], ( = 1 or 0) and free TAC ligand.
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http://dx.doi.org/10.1021/acs.inorgchem.2c03539 | DOI Listing |
J Comput Chem
April 2024
Department of Chemistry, Indian Institute of Technology Madras, Chennai, India.
The inability of p-block elements to participate in π-backbonding restricts them from activating small molecules like CO, H , and so forth. However, the development of the main group metallomimetics became a new pathway, where the main-group elements like boron can bind and activate small molecules like CO and H . The concept of the frustrated Lewis pair, Boron-Boron multiple bonds, and borylene are previously illustrated.
View Article and Find Full Text PDFChemistry
February 2024
Department of Chemistry, Indian Institute of Technology Madras, Chennai, 600036, India.
Researchers have successfully isolated Si /Ge species, termed silylone and germylone, with two lone pairs of electrons on them. These elusive compounds have been stabilised in singlet ground states by using different donor base ligands. Driess et al.
View Article and Find Full Text PDFJ Comput Chem
July 2023
Department of Chemistry, Indian Institute of Technology Madras, Chennai, India.
Stabilizing the exotic chemical species possessing multiple bonds is often extremely challenging due to insufficient orbital overlap, especially involving one heavier element. Bulky aryl groups and/or carbene as ligand have previously stabilized the SiSi, GeGe, and BB triple bonds. Herein, theoretical calculations have been carried out to shed light on the stability and bonding of elusive silaboryne/germaboryne (Si/GeB triple bond) stabilized by donor base ligands ((cAAC)BE(Me)(L); E = Si, L = cAAC , NHC , PMe ; E = Ge, L = cAAC ).
View Article and Find Full Text PDFInorg Chem
March 2023
Department of Chemistry, University of Bath, Bath BA2 7AY, U.K.
A family of zinc phosphate complexes supported by nitrogen donor-base ligands have been synthesized, and their molecular structures were identified in both the solid (X-ray crystallography) and solution state (DOSY NMR spectroscopy). [Zn{OP(OPh)}] (), formed from the reaction of Zn[N(SiMe)] with HO(O)P(OPh) coordinates to donor-base ligands, , pyridine (Py), 4-methylpyridine (4-MePy), 2,2-bipyridine (bipy), tetramethylethylenediamine (TMEDA), pentamethyldiethylenetriamine (PMDETA), and 1,3,5-trimethyl-1,3,5-triazacyclohexane (Me-TAC), to produce polymeric 1D structures, [(Py)Zn{OP(OPh)}] () and [(4-MePy)Zn{OP(OPh)}] (), the bimetalic systems, [(Bipy)Zn{OP(OPh)}] (), [(TMEDA)Zn{OP(OPh)}] (), and [(Me-TAC)Zn{OP(OPh)}] (), as well as a mono-nuclear zinc bis-diphenylphosphate complex, [(PMDETA)Zn{OP(OPh)}] (). H NMR DOSY has been used to calculate averaged molecular weights of the species.
View Article and Find Full Text PDFGallium phosphide is a three-dimensional polymeric material of the hetero-diatomic GaP unit, which has a wurtzite type structure, and captivating application as a light emitting diode (LED). As a result, there is a constant search for suitable precursors to synthesise GaP-based materials. However, the corresponding monomeric species is exotic in nature due to the expected Ga[triple bond, length as m-dash]P multiple bond.
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