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Design, synthesis, and Evaluation of Unsymmetrical Difluoro-Boron Complexes with Imidazoline as Potential Fungicides

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Indexed by:期刊论文

Date of Publication:2009-01-01

Journal:HETEROATOM CHEMISTRY

Included Journals:SCIE、EI、Scopus

Volume:20

Issue:7

Page Number:418-424

ISSN No.:1042-7163

Abstract:A series of unsymmetrical difluoroboron(BF(2)) complexes with pyridine and imidazoline were synthesized by reaction of new chelating ligands (arylmethyl-imidazolidinylidene)-pyridin-2-yl-amine with boron trifluoride diethyl etherate. All the ligands and BF(2) complexes were structurally characterized by IR, HRMS,(1)H, (13)C, (11)B, and (19)F NMR, indicating the bidentate complexation of imidazoline nitrogen and the pyridine nitrogen to the boron center. Evaluation of agricultural bioactivities showed that some of the BF(2) complexes exhibited moderate fungicidal activities, and most of the BF(2) complexes exhibited higher activities than the none-BF(2) complexed substrates. (C) 2010 Wiley Periodicals, Inc. Heteroatom Chem 20:418-424, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20567

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