Synthesis, characterization and antifungal studies of arylspiroborates derived from 4-nitrocatechol

Joseph A. Mosseler; Jennifer A. Melanson; Eric G. Bowes; Graham M. Lee; Christopher M. Vogels; Felix J. Baerlocher; Andreas Decken; Stephen A. Westcott

doi:10.1016/j.molstruc.2011.06.034

Synthesis, characterization and antifungal studies of arylspiroborates derived from 4-nitrocatechol

Joseph A. Mosseler
, Jennifer A. Melanson
, Eric G. Bowes
, Graham M. Lee
, Christopher M. Vogels
, Felix J. Baerlocher
, Andreas Decken
, Stephen A. Westcott

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

6 Scopus citations

Abstract

A family of arylspiroborates has been prepared by the addition of 4-nitrocatechol, boric acid and either an alkali metal hydroxide or an ammonium hydroxide. All compounds were characterized fully using multinuclear NMR spectroscopy, FT-IR spectroscopy and by elemental analyses. A single crystal X-ray diffraction was carried out on triethylmethylammonium 4-nitro[1,2- benzenediolato(2-)-O,O′]borate (5). All new compounds were tested for potential fungicidal activity. © 2011 Elsevier B.V. All rights reserved.

Original language	English
Pages (from-to)	24-27
Number of pages	4
Journal	Journal of Molecular Structure
Volume	1002
Issue number	1-3
DOIs	https://doi.org/10.1016/j.molstruc.2011.06.034
State	Published - Sep 14 2011
Externally published	Yes

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10.1016/j.molstruc.2011.06.034

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@article{0c2a35edb6a7445490989c632121665e,

title = "Synthesis, characterization and antifungal studies of arylspiroborates derived from 4-nitrocatechol",

abstract = "A family of arylspiroborates has been prepared by the addition of 4-nitrocatechol, boric acid and either an alkali metal hydroxide or an ammonium hydroxide. All compounds were characterized fully using multinuclear NMR spectroscopy, FT-IR spectroscopy and by elemental analyses. A single crystal X-ray diffraction was carried out on triethylmethylammonium 4-nitro[1,2- benzenediolato(2-)-O,O′]borate (5). All new compounds were tested for potential fungicidal activity. {\textcopyright} 2011 Elsevier B.V. All rights reserved.",

author = "Mosseler, \{Joseph A.\} and Melanson, \{Jennifer A.\} and Bowes, \{Eric G.\} and Lee, \{Graham M.\} and Vogels, \{Christopher M.\} and Baerlocher, \{Felix J.\} and Andreas Decken and Westcott, \{Stephen A.\}",

year = "2011",

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day = "14",

doi = "10.1016/j.molstruc.2011.06.034",

language = "English",

volume = "1002",

pages = "24--27",

journal = "Journal of Molecular Structure",

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publisher = "Elsevier B.V.",

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TY - JOUR

T1 - Synthesis, characterization and antifungal studies of arylspiroborates derived from 4-nitrocatechol

AU - Mosseler, Joseph A.

AU - Melanson, Jennifer A.

AU - Bowes, Eric G.

AU - Lee, Graham M.

AU - Vogels, Christopher M.

AU - Baerlocher, Felix J.

AU - Decken, Andreas

AU - Westcott, Stephen A.

PY - 2011/9/14

Y1 - 2011/9/14

N2 - A family of arylspiroborates has been prepared by the addition of 4-nitrocatechol, boric acid and either an alkali metal hydroxide or an ammonium hydroxide. All compounds were characterized fully using multinuclear NMR spectroscopy, FT-IR spectroscopy and by elemental analyses. A single crystal X-ray diffraction was carried out on triethylmethylammonium 4-nitro[1,2- benzenediolato(2-)-O,O′]borate (5). All new compounds were tested for potential fungicidal activity. © 2011 Elsevier B.V. All rights reserved.

AB - A family of arylspiroborates has been prepared by the addition of 4-nitrocatechol, boric acid and either an alkali metal hydroxide or an ammonium hydroxide. All compounds were characterized fully using multinuclear NMR spectroscopy, FT-IR spectroscopy and by elemental analyses. A single crystal X-ray diffraction was carried out on triethylmethylammonium 4-nitro[1,2- benzenediolato(2-)-O,O′]borate (5). All new compounds were tested for potential fungicidal activity. © 2011 Elsevier B.V. All rights reserved.

UR - https://www.scopus.com/pages/publications/80052274162

U2 - 10.1016/j.molstruc.2011.06.034

DO - 10.1016/j.molstruc.2011.06.034

M3 - Article

SN - 0022-2860

VL - 1002

SP - 24

EP - 27

JO - Journal of Molecular Structure

JF - Journal of Molecular Structure

IS - 1-3

ER -

Synthesis, characterization and antifungal studies of arylspiroborates derived from 4-nitrocatechol

Abstract

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