Synthesis, Characterization and Antimicrobial Activities of Pentacyclic Oxadiazadiborinanes

Detalhes bibliográficos
Autor(a) principal: Gormley,Patrick T.
Data de Publicação: 2020
Outros Autores: Geier,Stephen J., Vogels,Christopher M., Khuong,B. Ninh, MacCormack,Tyson J., Masuda,Jason D., Westcott,Stephen A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532020000701541
Resumo: In this study we have expanded upon a family of substituted pentacyclic oxadiazadiborinane derivatives from the condensation of carbohydrazide with ortho-formylphenyl boronic acid derivatives containing a variety of chemical and physical properties. All new complexes have been characterized fully including two single crystal X-ray diffraction studies which confirm the solid-state structure of these species along with an unusual methanol activation product, which appears to be a minor solid-state side product. The lack of inherent solubility of these compounds in common physiological media precluded us from doing traditional antimicrobial activities. To circumvent this problem, we incorporated these boron compounds into chitosan films. Only weak or moderate activities against Gram-negative and Gram-positive bacteria were observed in this study.
id SBQ-2_92ee3b04fd874397ce7293edf4065782
oai_identifier_str oai:scielo:S0103-50532020000701541
network_acronym_str SBQ-2
network_name_str Journal of the Brazilian Chemical Society (Online)
repository_id_str
spelling Synthesis, Characterization and Antimicrobial Activities of Pentacyclic OxadiazadiborinanesantimicrobialboronchitosanheterocyclicX-ray diffractionIn this study we have expanded upon a family of substituted pentacyclic oxadiazadiborinane derivatives from the condensation of carbohydrazide with ortho-formylphenyl boronic acid derivatives containing a variety of chemical and physical properties. All new complexes have been characterized fully including two single crystal X-ray diffraction studies which confirm the solid-state structure of these species along with an unusual methanol activation product, which appears to be a minor solid-state side product. The lack of inherent solubility of these compounds in common physiological media precluded us from doing traditional antimicrobial activities. To circumvent this problem, we incorporated these boron compounds into chitosan films. Only weak or moderate activities against Gram-negative and Gram-positive bacteria were observed in this study.Sociedade Brasileira de Química2020-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532020000701541Journal of the Brazilian Chemical Society v.31 n.7 2020reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20200040info:eu-repo/semantics/openAccessGormley,Patrick T.Geier,Stephen J.Vogels,Christopher M.Khuong,B. NinhMacCormack,Tyson J.Masuda,Jason D.Westcott,Stephen A.eng2020-06-30T00:00:00Zoai:scielo:S0103-50532020000701541Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2020-06-30T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Synthesis, Characterization and Antimicrobial Activities of Pentacyclic Oxadiazadiborinanes
title Synthesis, Characterization and Antimicrobial Activities of Pentacyclic Oxadiazadiborinanes
spellingShingle Synthesis, Characterization and Antimicrobial Activities of Pentacyclic Oxadiazadiborinanes
Gormley,Patrick T.
antimicrobial
boron
chitosan
heterocyclic
X-ray diffraction
title_short Synthesis, Characterization and Antimicrobial Activities of Pentacyclic Oxadiazadiborinanes
title_full Synthesis, Characterization and Antimicrobial Activities of Pentacyclic Oxadiazadiborinanes
title_fullStr Synthesis, Characterization and Antimicrobial Activities of Pentacyclic Oxadiazadiborinanes
title_full_unstemmed Synthesis, Characterization and Antimicrobial Activities of Pentacyclic Oxadiazadiborinanes
title_sort Synthesis, Characterization and Antimicrobial Activities of Pentacyclic Oxadiazadiborinanes
author Gormley,Patrick T.
author_facet Gormley,Patrick T.
Geier,Stephen J.
Vogels,Christopher M.
Khuong,B. Ninh
MacCormack,Tyson J.
Masuda,Jason D.
Westcott,Stephen A.
author_role author
author2 Geier,Stephen J.
Vogels,Christopher M.
Khuong,B. Ninh
MacCormack,Tyson J.
Masuda,Jason D.
Westcott,Stephen A.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Gormley,Patrick T.
Geier,Stephen J.
Vogels,Christopher M.
Khuong,B. Ninh
MacCormack,Tyson J.
Masuda,Jason D.
Westcott,Stephen A.
dc.subject.por.fl_str_mv antimicrobial
boron
chitosan
heterocyclic
X-ray diffraction
topic antimicrobial
boron
chitosan
heterocyclic
X-ray diffraction
description In this study we have expanded upon a family of substituted pentacyclic oxadiazadiborinane derivatives from the condensation of carbohydrazide with ortho-formylphenyl boronic acid derivatives containing a variety of chemical and physical properties. All new complexes have been characterized fully including two single crystal X-ray diffraction studies which confirm the solid-state structure of these species along with an unusual methanol activation product, which appears to be a minor solid-state side product. The lack of inherent solubility of these compounds in common physiological media precluded us from doing traditional antimicrobial activities. To circumvent this problem, we incorporated these boron compounds into chitosan films. Only weak or moderate activities against Gram-negative and Gram-positive bacteria were observed in this study.
publishDate 2020
dc.date.none.fl_str_mv 2020-07-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532020000701541
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532020000701541
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20200040
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.31 n.7 2020
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
_version_ 1750318183092322304