4.3 Article

Screening of fluorinated materials degrading microbes

Journal

JOURNAL OF FLUORINE CHEMISTRY
Volume 130, Issue 4, Pages 434-437

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jfluchem.2009.02.004

Keywords

Biodegradation; Bacterial strain; 16S rDNA sequence; Phylogeny

Ask authors/readers for more resources

Isolation of bacterial strains capable of degrading fluorinated materials was described. 8 strains of Actinobacteria exhibited degradability of ethyl difluoroacetate (DFAc) was accumulated by bacteria, giving difluoroacetic acid and then fluoride ion. Further, 13 strains of Actinobacteria exhibited degradability of fluorobenzene and/or benzotrifluoride. In batch culture, growth of strains on fluorinated materials led to the release of fluoride ion. (C) 2009 Published by Elsevier B.V.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
Article Chemistry, Inorganic & Nuclear

Iron-catalyzed sulfur alkylation of sulfenamides with in situ-generated 2,2,2-trifluorodiazoethane

Xianda Wu, Minghong Chen, Shuiyun Zheng, Fu-Sheng He, Jie Wu

Summary: Here, we report a new method for synthesizing sulfilimines through an iron-catalyzed reaction between sulfenamides and 2,2,2-trifluor-diazoethane. This protocol features operational simplicity, mild conditions, and can be conducted in open air, providing a facile approach to trifloromethylated sulfilimines in moderate to good yields.

JOURNAL OF FLUORINE CHEMISTRY (2024)

Article Chemistry, Inorganic & Nuclear

Regioselective synthesis of 3H-Pyrazoles bearing difluoromethyl phosphonate group

Ita Hajdin, Romana Pajkert, Haibo Mei, Jianlin Han, Gerd-Volker Roeschenthaler

Summary: A catalyst- and solvent-free 1,3-dipolar cycloaddition reaction using a bench-stable diazo reagent has been developed to obtain a series of novel 3H-pyrazoles bearing difluoromethyl phosphonate unit in moderate-to-excellent yields. This method provides an efficient and easy route to synthesize valuable compounds.

JOURNAL OF FLUORINE CHEMISTRY (2024)