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Chlorfenapyr Crystal Polymorphism and Insecticidal Activity.
Aronin, Reese; Brázda, Petr; Smith, Leilani N; Zhang, Carolyn Jin; Benedict, Jason B; Marr, Zoe Y; Rybtchinski, Boris; Weissman, Haim; Shtukenberg, Alexander G; Kahr, Bart.
Afiliação
  • Aronin R; Department of Chemistry and Molecular Design Institute, New York University, 29 Washington Place, New York City, New York 10003, United States.
  • Brázda P; Department of Structure Analysis, Institute of Physics, Czech Academy of Sciences, Na Slovance 2/1999 Prague 8, Prague 18221, Czech Republic.
  • Smith LN; Department of Chemistry and Molecular Design Institute, New York University, 29 Washington Place, New York City, New York 10003, United States.
  • Zhang CJ; Department of Chemistry and Molecular Design Institute, New York University, 29 Washington Place, New York City, New York 10003, United States.
  • Benedict JB; Department of Chemistry, University at Buffalo, Buffalo, New York 14260-3000, United States.
  • Marr ZY; Department of Chemistry, University at Buffalo, Buffalo, New York 14260-3000, United States.
  • Rybtchinski B; Department of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 76100, Israel.
  • Weissman H; Department of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 76100, Israel.
  • Shtukenberg AG; Department of Chemistry and Molecular Design Institute, New York University, 29 Washington Place, New York City, New York 10003, United States.
  • Kahr B; Department of Chemistry and Molecular Design Institute, New York University, 29 Washington Place, New York City, New York 10003, United States.
Cryst Growth Des ; 24(3): 1284-1292, 2024 Feb 07.
Article em En | MEDLINE | ID: mdl-38344671
ABSTRACT
Four crystalline polymorphs of the proinsecticide chlorfenapyr [4-bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-trifluoromethyl-1H-pyrrole-3-carbonitrile] have been identified and characterized by polarized light optical microscopy, differential scanning calorimetry, Raman spectroscopy, X-ray diffraction, and electron diffraction. Three of the four structures were considered polytypic. Chlorfenapyr polymorphs show similar lethality against fruit flies (Drosophila melanogaster) and mosquitoes (Anopheles quadrimaculatus) with the least stable polymorph showing slightly higher lethality. Similar activities may be expected to be consistent with structural similarities. Knockdown kinetics, however, depend on an internal metabolic activating step, which further complicates polymorph-dependent bioavailability.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Cryst Growth Des Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Cryst Growth Des Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos