Publications by authors named "Chhotan Mandal"

Article Synopsis
  • Heteroleptic magnesium hydrides (MgH) are key in chemistry for their ability to facilitate stoichiometric and catalytic reductions, with hydride acting as the main reactive site, while additional ligands often play a passive role.
  • Recent research by Milstein introduced a new alkyne hydrogenation method that uses a non-innocent PNP pincer ligand in combination with MgH, although without confirming its structure.
  • This study presents a novel NNN-chelator with a dearomatized picolyl group that creates a well-defined MgH capable of reacting with various electrophiles, showing differences in reactivity toward nonpolar alkynes versus polar carbonyls.
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Molecular magnesium hydrides and hydride-rich clusters are of significant interest for applications ranging from catalysis and small molecule activation to hydrogen storage. Here, we investigate the 2-anilidomethylpyridine framework L as an ancillary support for magnesium organometallics with a special emphasis on hydrides. The proligand L (-[2,6-bis(1-methylethyl)phenyl]-α,6-diphenyl-2-pyridinemethanamine) gives [(L)Mg(Bu)(thf)] () by butane elimination from Mg(Bu)(thf).

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Exclusive C-donating ligands are rarely used with kinetically labile heavier alkaline earths (Ca, Sr, Ba). We report herein the aptitude of a combination of NHC with fluorenyl connected by a flexible -(CH)- linker as a ligand support for heteroleptic Ca- and Sr-N(SiMe) and iodides. The Ca-N(SiMe) complex even catalyzes the intramolecular hydroamination of aminoalkenes to showcase the effectiveness of this ligand framework.

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Low-coordinate heteroleptic zinc hydrides are catalytically important but rare and synthetically challenging. We herein report three-coordinate monomeric zinc hydride on a 2-anilidomethylpyridine framework (L). The synthetic success comes through systematically screening a few different routes from different precursors.

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Dearomatized 1,4-dihydropyridyl motifs are significant in both chemistry and biology for their potential abilities to deliver the stored hydride, driven by rearomatization. Biological cofactors like nicotinamide adenine dinucleotide (NADH) and organic 'hydride sources' like Hantzsch esters are prime examples. An organoaluminum chemistry on a 2-anilidomethylpyridine framework is reported, where such hydride storage and transfer abilities are displayed by the ligand's pyridyl unit.

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The electron-rich cyclopentadienyl and the analogous indenyl and fluorenyl ligands (collectively denoted here as Cp') have been impactful in stabilizing electron-deficient metal centers including the highly electropositive alkaline earths. Being in the s-block, the group 2 metals follow a major periodic variation in their atomic and ionic properties which is reflected in those Cp' compounds. This article presents an overview of this class of compounds for all the five metals from beryllium to barium (radium is excluded for its radioactivity), highlighting their systematic variation.

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