Synthesis and structural studies of three-dimensional supramolecular motifs derived from neutral and cationic zinc alkanesulfonates

Ravi Shankar; Rohit Singh; Swati Mendiratta; Amanpreet Kaur Jassal; Gabriele Kociok-Kohn; Kieran C. Molloy

doi:10.1002/ejic.201601320

Synthesis and structural studies of three-dimensional supramolecular motifs derived from neutral and cationic zinc alkanesulfonates

Ravi Shankar, Rohit Singh, Swati Mendiratta, Amanpreet Kaur Jassal, Gabriele Kociok-Kohn, Kieran C. Molloy

Indian Institute of Technology Kanpur

Research output: Contribution to journal › Article › peer-review

7 Citations (SciVal)

Abstract

The one-pot reactions between anhydrous zinc acetate, diethyl or di-n-propyl sulfite, and tetraalkylammonium iodide (120 °C, 12 h) proceed through sulfur-centered Arbuzov-type rearrangement to afford [R¹ ₄N]₂[Zn(OSO₂R)₄] [R¹, R = Et (1); R¹ = nBu, R = nPr (2)] bearing alkanesulfonate groups bound to the metal center. The zincate salts 1 and 2 are used as precursors for the synthesis of neutral and cationic coordination complexes, namely, [Zn(OSO₂Et)₂(bipy)(dmso)₂] (3; bipy = 4,4'-bipyridine, dmso = dimethyl sulfoxide), [Zn(OSO₂nPr)₂(bipy)₂]·dmso·H₂O (4), [Zn(bipy)(H₂O)₄](OSO₂Et)₂ (5), [Zn(H₂O)₆](OSO₂Et)₂ (6), and [Zn(H₂O)₆](OSO₂nPr)₂ (7). X-ray crystallographic studies of 3-7 reveal that the alkanesulfonate groups act as prolific H-bond acceptors and assist the transformation of zero-, one-, or two-dimensional coordination frameworks into three-dimensional structural motifs.

Original language	English
Pages (from-to)	2081–2087
Journal	European Journal of Inorganic Chemistry
Volume	2017
Issue number	14
DOIs	https://doi.org/10.1002/ejic.201601320
Publication status	Published - 10 Apr 2017

Keywords

Alkanesulfonates
Hydrogen bonds
Structure elucidation
Supramolecular chemistry
Zincates

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10.1002/ejic.201601320

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title = "Synthesis and structural studies of three-dimensional supramolecular motifs derived from neutral and cationic zinc alkanesulfonates",

abstract = "The one-pot reactions between anhydrous zinc acetate, diethyl or di-n-propyl sulfite, and tetraalkylammonium iodide (120 °C, 12 h) proceed through sulfur-centered Arbuzov-type rearrangement to afford [R1 4N]2[Zn(OSO2R)4] [R1, R = Et (1); R1 = nBu, R = nPr (2)] bearing alkanesulfonate groups bound to the metal center. The zincate salts 1 and 2 are used as precursors for the synthesis of neutral and cationic coordination complexes, namely, [Zn(OSO2Et)2(bipy)(dmso)2] (3; bipy = 4,4'-bipyridine, dmso = dimethyl sulfoxide), [Zn(OSO2nPr)2(bipy)2]·dmso·H2O (4), [Zn(bipy)(H2O)4](OSO2Et)2 (5), [Zn(H2O)6](OSO2Et)2 (6), and [Zn(H2O)6](OSO2nPr)2 (7). X-ray crystallographic studies of 3-7 reveal that the alkanesulfonate groups act as prolific H-bond acceptors and assist the transformation of zero-, one-, or two-dimensional coordination frameworks into three-dimensional structural motifs.",

keywords = "Alkanesulfonates, Hydrogen bonds, Structure elucidation, Supramolecular chemistry, Zincates",

author = "Ravi Shankar and Rohit Singh and Swati Mendiratta and Jassal, {Amanpreet Kaur} and Gabriele Kociok-Kohn and Molloy, {Kieran C.}",

year = "2017",

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language = "English",

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T1 - Synthesis and structural studies of three-dimensional supramolecular motifs derived from neutral and cationic zinc alkanesulfonates

AU - Shankar, Ravi

AU - Singh, Rohit

AU - Mendiratta, Swati

AU - Jassal, Amanpreet Kaur

AU - Kociok-Kohn, Gabriele

AU - Molloy, Kieran C.

PY - 2017/4/10

Y1 - 2017/4/10

N2 - The one-pot reactions between anhydrous zinc acetate, diethyl or di-n-propyl sulfite, and tetraalkylammonium iodide (120 °C, 12 h) proceed through sulfur-centered Arbuzov-type rearrangement to afford [R1 4N]2[Zn(OSO2R)4] [R1, R = Et (1); R1 = nBu, R = nPr (2)] bearing alkanesulfonate groups bound to the metal center. The zincate salts 1 and 2 are used as precursors for the synthesis of neutral and cationic coordination complexes, namely, [Zn(OSO2Et)2(bipy)(dmso)2] (3; bipy = 4,4'-bipyridine, dmso = dimethyl sulfoxide), [Zn(OSO2nPr)2(bipy)2]·dmso·H2O (4), [Zn(bipy)(H2O)4](OSO2Et)2 (5), [Zn(H2O)6](OSO2Et)2 (6), and [Zn(H2O)6](OSO2nPr)2 (7). X-ray crystallographic studies of 3-7 reveal that the alkanesulfonate groups act as prolific H-bond acceptors and assist the transformation of zero-, one-, or two-dimensional coordination frameworks into three-dimensional structural motifs.

AB - The one-pot reactions between anhydrous zinc acetate, diethyl or di-n-propyl sulfite, and tetraalkylammonium iodide (120 °C, 12 h) proceed through sulfur-centered Arbuzov-type rearrangement to afford [R1 4N]2[Zn(OSO2R)4] [R1, R = Et (1); R1 = nBu, R = nPr (2)] bearing alkanesulfonate groups bound to the metal center. The zincate salts 1 and 2 are used as precursors for the synthesis of neutral and cationic coordination complexes, namely, [Zn(OSO2Et)2(bipy)(dmso)2] (3; bipy = 4,4'-bipyridine, dmso = dimethyl sulfoxide), [Zn(OSO2nPr)2(bipy)2]·dmso·H2O (4), [Zn(bipy)(H2O)4](OSO2Et)2 (5), [Zn(H2O)6](OSO2Et)2 (6), and [Zn(H2O)6](OSO2nPr)2 (7). X-ray crystallographic studies of 3-7 reveal that the alkanesulfonate groups act as prolific H-bond acceptors and assist the transformation of zero-, one-, or two-dimensional coordination frameworks into three-dimensional structural motifs.

KW - Alkanesulfonates

KW - Hydrogen bonds

KW - Structure elucidation

KW - Supramolecular chemistry

KW - Zincates

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UR - http://dx.doi.org/10.1002/ejic.201601320

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DO - 10.1002/ejic.201601320

M3 - Article

AN - SCOPUS:85013371950

SN - 1434-1948

VL - 2017

SP - 2081

EP - 2087

JO - European Journal of Inorganic Chemistry

JF - European Journal of Inorganic Chemistry

IS - 14

ER -

Synthesis and structural studies of three-dimensional supramolecular motifs derived from neutral and cationic zinc alkanesulfonates

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Keywords

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Synthesis and structural studies of three-dimensional supramolecular motifs derived from neutral and cationic zinc alkanesulfonates

Abstract

Keywords

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