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Title: Syntheses, structures, and 1H, 13C{1H} and 119Sn{1H} NMR chemical shifts of a family of trimethyltin alkoxide, amide, halide and cyclopentadienyl compounds

Abstract

The synthesis and full characterization, including Nuclear Magnetic Resonance (NMR) data (1H, 13C{1H} and 119Sn{1H}), for a series of Me3SnX (X = O-2,6-tBu2C6H3 (1), (Me3Sn)N(2,6-iPr2C6H3) (3), NH-2,4,6-tBu3C6H2 (4), N(SiMe3)2 (5), NEt2, C5Me5 (6), Cl, Br, I, and SnMe3) compounds in benzene-d6, toluene-d8, dichloromethane-d2, chloroform-d1, acetonitrile-d3, and tetrahydrofuran-d8 are reported. The X-ray crystal structures of Me3Sn(O-2,6-tBu2C6H3) (1), Me3Sn(O-2,6-iPr2C6H3) (2), and (Me3Sn)(NH-2,4,6-tBu3C6H2) (4) are also presented. As a result, these compiled data complement existing literature data and ease the characterization of these compounds by routine NMR experiments.

Authors:
 [1];  [1];  [1];  [1];  [1]
  1. Los Alamos National Lab. (LANL), Los Alamos, NM (United States)
Publication Date:
Research Org.:
Los Alamos National Lab. (LANL), Los Alamos, NM (United States)
Sponsoring Org.:
USDOE Laboratory Directed Research and Development (LDRD) Program
OSTI Identifier:
1329685
Report Number(s):
LA-UR-15-23489
Journal ID: ISSN 1477-9226; ICHBD9
Grant/Contract Number:  
AC52-06NA25396
Resource Type:
Accepted Manuscript
Journal Name:
Dalton Transactions
Additional Journal Information:
Journal Volume: 44; Journal Issue: 36; Journal ID: ISSN 1477-9226
Publisher:
Royal Society of Chemistry
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY

Citation Formats

Lichtscheidl, Alejandro G., Janicke, Michael T., Scott, Brian L., Nelson, Andrew T., and Kiplinger, Jaqueline L. Syntheses, structures, and 1H, 13C{1H} and 119Sn{1H} NMR chemical shifts of a family of trimethyltin alkoxide, amide, halide and cyclopentadienyl compounds. United States: N. p., 2015. Web. doi:10.1039/C5DT01980J.
Lichtscheidl, Alejandro G., Janicke, Michael T., Scott, Brian L., Nelson, Andrew T., & Kiplinger, Jaqueline L. Syntheses, structures, and 1H, 13C{1H} and 119Sn{1H} NMR chemical shifts of a family of trimethyltin alkoxide, amide, halide and cyclopentadienyl compounds. United States. doi:10.1039/C5DT01980J.
Lichtscheidl, Alejandro G., Janicke, Michael T., Scott, Brian L., Nelson, Andrew T., and Kiplinger, Jaqueline L. Fri . "Syntheses, structures, and 1H, 13C{1H} and 119Sn{1H} NMR chemical shifts of a family of trimethyltin alkoxide, amide, halide and cyclopentadienyl compounds". United States. doi:10.1039/C5DT01980J. https://www.osti.gov/servlets/purl/1329685.
@article{osti_1329685,
title = {Syntheses, structures, and 1H, 13C{1H} and 119Sn{1H} NMR chemical shifts of a family of trimethyltin alkoxide, amide, halide and cyclopentadienyl compounds},
author = {Lichtscheidl, Alejandro G. and Janicke, Michael T. and Scott, Brian L. and Nelson, Andrew T. and Kiplinger, Jaqueline L.},
abstractNote = {The synthesis and full characterization, including Nuclear Magnetic Resonance (NMR) data (1H, 13C{1H} and 119Sn{1H}), for a series of Me3SnX (X = O-2,6-tBu2C6H3 (1), (Me3Sn)N(2,6-iPr2C6H3) (3), NH-2,4,6-tBu3C6H2 (4), N(SiMe3)2 (5), NEt2, C5Me5 (6), Cl, Br, I, and SnMe3) compounds in benzene-d6, toluene-d8, dichloromethane-d2, chloroform-d1, acetonitrile-d3, and tetrahydrofuran-d8 are reported. The X-ray crystal structures of Me3Sn(O-2,6-tBu2C6H3) (1), Me3Sn(O-2,6-iPr2C6H3) (2), and (Me3Sn)(NH-2,4,6-tBu3C6H2) (4) are also presented. As a result, these compiled data complement existing literature data and ease the characterization of these compounds by routine NMR experiments.},
doi = {10.1039/C5DT01980J},
journal = {Dalton Transactions},
number = 36,
volume = 44,
place = {United States},
year = {2015},
month = {8}
}

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    Works referencing / citing this record:

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    • Fulmer, Gregory R.; Miller, Alexander J. M.; Sherden, Nathaniel H.
    • Organometallics, Vol. 29, Issue 9
    • DOI: 10.1021/om100106e

    Synthesis of 1-Stannacyclopent-3-enes and Their Pyrolysis to Stannylenes
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    • Zhou, Dong; Reiche, Clemens; Nag, Mrinmoy
    • Organometallics, Vol. 28, Issue 8
    • DOI: 10.1021/om800541f

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