ItemArticle

Assembly of discrete and oligomeric structures of organotin double-decker silsesquioxanes: Inherent stability studies

Title
Assembly of discrete and oligomeric structures of organotin double-decker silsesquioxanes: Inherent stability studies
Creator
Loganathan P.; Pillai R.S.; Jeevananthan V.; David E.; Palanisami N.; Bhuvanesh N.S.P.; Shanmugan S.
Description
Double-decker silsesquioxane (DDSQ), a type of incompletely condensed silsesquioxane, has been used as a molecular precursor for synthesizing new organotin discrete and oligomeric compounds. The equimolar reaction between DDSQ tetrasilanol (DDSQ-4OH) and Ph2SnCl2 in the presence of triethylamine leads to obtaining discrete [Ph4Sn2O4(DDSQ)(THF)2] (1). The change of sterically bulky aryl Ph2SnCl2 precursor to linear alkyl nBu2SnCl2 led to the isolation of oligomeric [nBu4Sn2O4(DDSQ)] (2). The structures of compounds 1 and 2 have been demonstrated using single-crystal X-ray diffraction measurements. Indeed, the formation of oligomeric organotin DDSQ compound (2) was determined using GPC and MALDI-TOF mass spectroscopy. In compound 1, the geometry of the tin atom is five-coordinated trigonal bipyramidal by two phenyl groups, two Si-O from DDSQ and one tetrahydrofuran. Compound 2 contains four coordinated two peripheral tin atoms and two five-coordinated central tin atoms, in which, the fifth coordinating oxo groups in the central tin atoms create the bridge between two different DDSQ units that leads to the formation of oligomeric structure. Density functional theory calculations on organotin DDSQs infer that the obtained lattice energy for compound 1 is far higher than for the case of compound 2, which indicates that the crystal of compound 1 is better stabilized in its crystal lattice with stronger close packing via intermolecular interactions between discrete molecules with coordinated THF compared to the crystal of compound 2. The greater stability arises mainly due to the sterically bulkier phenyl groups attached to the tin centers in compound 1, which provide accessibility for accommodating the THF molecule per tin via Sn-THF bonding, while contrarily the smaller n-butyl groups aid the polymerization of the four repeating units of [SnSi4O7] or two Sn2O4(DDSQ) through ?-oxo groups. Both compounds 1 and 2 were chosen to be promising precursors for the synthesis of ceramic tin silicates. The thermolysis of 2 at 1000 C afforded the mixture of crystalline SnSiO4 and SiO2 but the same mixture was only formed by thermolysis of 1 at relatively higher temperature (1500 C), which infers that compound 1 is more stable than compound 2 that is in good synergy with theoretical lattice energy. The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
Source
New Journal of Chemistry, Vol-45, No. 43, pp. 20144-20154.
Date
2021-01-01
Publisher
Royal Society of Chemistry
Coverage
Loganathan P., Department of Chemistry, Faculty of Engineering and Technology, SRM Institute of Science and Technology, Tamil Nadu, Kattankulathur, 603203, India; Pillai R.S., Department of Chemistry, Faculty of Engineering and Technology, SRM Institute of Science and Technology, Tamil Nadu, Kattankulathur, 603203, India, Department of Chemistry, Christ University, Karnataka, Bangalore, 56029, India; Jeevananthan V., Department of Chemistry, Faculty of Engineering and Technology, SRM Institute of Science and Technology, Tamil Nadu, Kattankulathur, 603203, India; David E., Centre for Functional Materials, Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Tamil Nadu, Vellore, 632014, India; Palanisami N., Centre for Functional Materials, Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Tamil Nadu, Vellore, 632014, India; Bhuvanesh N.S.P., X-ray Diffraction Laboratory, Department of Chemistry, Texas AandM University, College Station, 77842, TX, United States; Shanmugan S., Department of Chemistry, Faculty of Engineering and Technology, SRM Institute of Science and Technology, Tamil Nadu, Kattankulathur, 603203, India
Rights
Restricted Access
Relation
ISSN: 11440546; CODEN: NJCHE
Format
Online
Language
English
Type
Article

Collection

Articles

Citation

Loganathan P.; Pillai R.S.; Jeevananthan V.; David E.; Palanisami N.; Bhuvanesh N.S.P.; Shanmugan S., “Assembly of discrete and oligomeric structures of organotin double-decker silsesquioxanes: Inherent stability studies,” CHRIST (Deemed To Be University) Institutional Repository, accessed March 19, 2025, https://archives.christuniversity.in/items/show/15627.

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