Pyridylpyrrolido ligand in Ge(II) and Sn(II) chemistry: synthesis, reactivity and catalytic application
Title | Pyridylpyrrolido ligand in Ge(II) and Sn(II) chemistry: synthesis, reactivity and catalytic application |
Publication Type | Journal Article |
Year of Publication | 2021 |
Authors | Pahar, S, Sharma, V, Tothadi, S, Sen, SS |
Journal | Dalton Transactions |
Volume | 50 |
Issue | 45 |
Pagination | 16678-16684 |
Date Published | NOV |
Type of Article | Article |
ISSN | 1477-9226 |
Abstract | In our previous communication, we have reported the synthesis of a new chlorogermylene (B) featuring a pyridylpyrrolido ligand. This study details the preparation of a series of new germylenes and stannylenes starting from B. A transmetallation reaction between B and SnCl2 led to the analogous chlorostannylene (1) with the simultaneous elimination of GeCl2. This is a very unusual example of transmetallation between two elements of the same group. The preparation of 1via lithiation led to the formation of 2 as a side product, where the ortho C-H bond of the pyridine ring was activated and functionalized with a Bu-n moiety. Subsequently, B and 1 were used as precursors to generate germylene (4) and stannylene (5) featuring tris(trimethylsilyl)silyl (hypersilyl) moieties. We also prepared tetrafluoropyridyl germylene (6) by reacting 4 with C5F5N with the simultaneous elimination of (Me3Si)(3)SiF by utilizing the fluoride affinity of the silicon atom. As there is scarcity of Sn(II) compounds as single-site catalysts, we investigated 5 as a catalyst towards the hydroboration of aldehydes, ketones, alkenes and alkynes. All the compounds have been characterized by single-crystal X-ray diffraction and by state of the art spectroscopic studies. |
DOI | 10.1039/d1dt03136h |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 4.390 |
Divison category:
Catalysis and Inorganic Chemistry
Organic Chemistry
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