Phosphonothioate Hydrolysis by Molybdocene Dichlorides: Importance of Metal Interaction with the Sulfur of the Thiolate Leaving Group
العنوان: | Phosphonothioate Hydrolysis by Molybdocene Dichlorides: Importance of Metal Interaction with the Sulfur of the Thiolate Leaving Group |
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المؤلفون: | Kristina M. Dill, Louis Y. Kuo, Adria K. Dortignacq, Devon C. Baker |
المصدر: | Organometallics. 32:4759-4765 |
بيانات النشر: | American Chemical Society (ACS), 2013. |
سنة النشر: | 2013 |
مصطلحات موضوعية: | inorganic chemicals, Aqueous solution, Organic Chemistry, Leaving group, chemistry.chemical_element, macromolecular substances, environment and public health, Phosphonate, Medicinal chemistry, Sulfur, Inorganic Chemistry, chemistry.chemical_compound, Hydrolysis, chemistry, Cyclopentadienyl complex, Organic chemistry, Physical and Theoretical Chemistry, Metallocene, Bond cleavage |
الوصف: | The metallocene bis(cyclopentadienyl)molybdenum(IV) dichloride Cp2MoCl2 hydrolyzes O,S-diethyl phenylphosphonothioate (1) with only P–S scission to yield a phosphonate under mild aqueous conditions. In terms of degrading phosphonothioate neurotoxins, exclusive cleavage of the P–S linkage is preferred, for P–O scission yields another toxic phosphonothioate. Structure–activity relationship studies were undertaken with various phosphonothioates to test the hypothesis for the exclusive P–S scission by Cp2Mo(aq). Kinetics data show that the rates of phosphonothioate hydrolysis correspond to the size of the alkanethiolate leaving group on treatment with Cp2MoCl2. This suggests that the exclusive P–S scission of 1 is due to the interaction between the thiophilic Cp2Mo with the sulfur site of the P–SR linkage. |
تدمد: | 1520-6041 0276-7333 |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_________::e7d276ee7b59379427e7ccf850d5ca3e https://doi.org/10.1021/om400382u |
رقم الأكسشن: | edsair.doi...........e7d276ee7b59379427e7ccf850d5ca3e |
قاعدة البيانات: | OpenAIRE |
تدمد: | 15206041 02767333 |
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