The structure–activity relationship of some hexacoordinated dimethyltin(IV) complexes of fluorinated β‐diketone/β‐diketones and sterically congested heterocyclic β‐diketones. (2nd June 2015)
- Record Type:
- Journal Article
- Title:
- The structure–activity relationship of some hexacoordinated dimethyltin(IV) complexes of fluorinated β‐diketone/β‐diketones and sterically congested heterocyclic β‐diketones. (2nd June 2015)
- Main Title:
- The structure–activity relationship of some hexacoordinated dimethyltin(IV) complexes of fluorinated β‐diketone/β‐diketones and sterically congested heterocyclic β‐diketones
- Authors:
- Sharma, Arti
Jain, Asha
Saxena, Sanjiv - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The study was focused on the <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">structure–activity relationship</named-content> of some newly synthesized hexacoordinated dimethyltin(IV) complexes of fluorinated β‐diketone/β‐diketones and sterically congested heterocyclic β‐diketones. These complexes were screened for their <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">antibacterial activity</named-content> against a Gram‐negative bacterium (<italic>Pseudomonas aeruginosa</italic>) and Gram‐positive bacteria (<italic>Streptomyces griseus</italic>, <italic>Staphylococcus aureus</italic>, <italic>Bacillus subtilis</italic>) and the results were compared with those of a standard antibacterial drug. Some of the complexes were also screened for their antifungal activity against various fungi (<italic>Aspergillus niger</italic>, <italic>A</italic>. <italic>flavus</italic>, <italic>Trichoderma viride</italic>, <italic>Fusarium oxysporum</italic>) and were found to be active. These new hexacoordinated complexes of dimethyltin(IV) were generated by reactions of dimethyltin(IV) dichloride and sodium salts of fluorinated β‐diketone/β‐diketones and sterically congested heterocyclic β‐diketones in 1:1:1 molar ratio in refluxing dry benzene. Plausible structures of these<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The study was focused on the <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">structure–activity relationship</named-content> of some newly synthesized hexacoordinated dimethyltin(IV) complexes of fluorinated β‐diketone/β‐diketones and sterically congested heterocyclic β‐diketones. These complexes were screened for their <named-content content-type="chemicalTechnology" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">antibacterial activity</named-content> against a Gram‐negative bacterium (<italic>Pseudomonas aeruginosa</italic>) and Gram‐positive bacteria (<italic>Streptomyces griseus</italic>, <italic>Staphylococcus aureus</italic>, <italic>Bacillus subtilis</italic>) and the results were compared with those of a standard antibacterial drug. Some of the complexes were also screened for their antifungal activity against various fungi (<italic>Aspergillus niger</italic>, <italic>A</italic>. <italic>flavus</italic>, <italic>Trichoderma viride</italic>, <italic>Fusarium oxysporum</italic>) and were found to be active. These new hexacoordinated complexes of dimethyltin(IV) were generated by reactions of dimethyltin(IV) dichloride and sodium salts of fluorinated β‐diketone/β‐diketones and sterically congested heterocyclic β‐diketones in 1:1:1 molar ratio in refluxing dry benzene. Plausible structures of these complexes were suggested with the aid of physicochemical and spectroscopic studies. <sup>119</sup>Sn NMR spectral data revealed the presence of a hexacoordinated tin centre in these dimethyltin(IV) complexes. Copyright © 2015 John Wiley &amp; Sons, Ltd.</p> </abstract> … (more)
- Is Part Of:
- Applied organometallic chemistry. Volume 29:Number 8(2015:Aug.)
- Journal:
- Applied organometallic chemistry
- Issue:
- Volume 29:Number 8(2015:Aug.)
- Issue Display:
- Volume 29, Issue 8 (2015)
- Year:
- 2015
- Volume:
- 29
- Issue:
- 8
- Issue Sort Value:
- 2015-0029-0008-0000
- Page Start:
- 499
- Page End:
- 508
- Publication Date:
- 2015-06-02
- Subjects:
- Organometallic chemistry -- Periodicals
Organometallic compounds -- Periodicals
547.05 - Journal URLs:
- http://www3.interscience.wiley.com/cgi-bin/jhome/109566206 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/2676 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/aoc.3321 ↗
- Languages:
- English
- ISSNs:
- 0268-2605
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1576.270000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3563.xml