Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Alagappan Thenappan"'
Publikováno v:
Journal of Polymer Science Part A: Polymer Chemistry
Journal of Polymer Science Part A: Polymer Chemistry, Wiley, 2014, 52, pp.1714-1720. ⟨10.1002/pola.27172⟩
Journal of Polymer Science Part A: Polymer Chemistry, Wiley, 2014, 52, pp.1714-1720. ⟨10.1002/pola.27172⟩
The radical copolymerization of chlorotrifluoroethylene (CTFE) with 3,3,4,4-tetrafluoro-4-bromobut-1-ene (BTFB) initiated by tert-butylperoxypivalate is presented. The microstructures of the obtained copolymers are determined by means of NMR spectros
Autor:
Chun Gao, Bruno Ameduri, Gérald Lopez, Peter L. Rinaldi, Linlin Li, Alagappan Thenappan, Faith J. Wyzgoski
Publikováno v:
Polymer Chemistry
Polymer Chemistry, Royal Society of Chemistry-RSC, 2015, 6, pp.3790-3799. ⟨10.1039/c5py00271k⟩
Polymer Chemistry, Royal Society of Chemistry-RSC, 2015, 6, pp.3790-3799. ⟨10.1039/c5py00271k⟩
International audience; The radical copolymerization of chlorotrifluoroethylene (CTFE) with vinylidene chloride (VDC) was investigated. A surfactant-free emulsion polymerization process was used to obtain poly(CTFE-co-VDC) copolymers of high molecula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79261b31577a1f82a10bd9638d4d82e6
https://hal.archives-ouvertes.fr/hal-01142700
https://hal.archives-ouvertes.fr/hal-01142700
Publikováno v:
ACS Macro Letters
ACS Macro Letters, Washington, D.C : American Chemical Society, 2014, 4, pp.16−20. ⟨10.1021/mz5006712⟩
ACS Macro Letters, Washington, D.C : American Chemical Society, 2014, 4, pp.16−20. ⟨10.1021/mz5006712⟩
Methods for the synthesis of CTFE-based block copolymers through iodine transfer polymerization are disclosed. In an exemplary embodiment, a method includes reacting a fluoromonomer "M" with a chain transfer agent of the formula X-Y or Y-X-Y, wherein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03464c91fb7caf61969f9419fc8c463d
https://hal.archives-ouvertes.fr/hal-01091808
https://hal.archives-ouvertes.fr/hal-01091808
Autor:
Donald J. Burton, Alagappan Thenappan
Publikováno v:
Journal of Fluorine Chemistry. 77:45-50
Fluorocarboethoxymethylene tri-n-butylphosphorane, Bu3P=CFCOOEt (3), reacts with per- and poly-fluoroalkyl-substituted carboxylic acid esters, ethyl formate and γ-butyrolactone to give the corresponding enol ethers, RFC (OEt)=CFCOOEt (4), in good yi
Autor:
Alagappan Thenappan, Harry S. Tung, Timothy R. Demmin, G. V. Bindu Madhavan, Michael Van Der Puy
Publikováno v:
Journal of Fluorine Chemistry. 76:49-54
1,1,1 -Trichlorotrifluoroethane was added to ethylene using the catalyst system Fe/triethylphosphite, which eliminated the need for a solvent and avoided the corrosion problems inherent in CuCl-catalyzed reactions. The adduct, CF 3 CCl 2 CH 2 CH 2 Cl
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 105:205-212
Acylation of [(EtO)2P(O)CFCO2Et]−Li+ 1 with acid chlorides RC(O)Cl or phosgene ClC(O)Cl and subsequent reaction of the acylated phosphonate with organometallic reagents (R'M) provide unsymmetrical and symmetrical tetrasubstituted α-fluoro-α,β-un
Publikováno v:
The Journal of Organic Chemistry. 59:7085-7091
Autor:
Donald J. Burton, Alagappan Thenappan
Publikováno v:
The Journal of Organic Chemistry. 56:273-277
(Fluorocarbethoxymethylene) tri-n-butylphosphorane (3) reacts with acid chlorides and anhydrides to form the corresponding carbon acylated phosphonium salts 4, and hydrolysis of 4 under mild basic conditions provides RCOCFHCOOEt (8) in moderate yield
Autor:
Donald J. Burton, Alagappan Thenappan
Publikováno v:
The Journal of Organic Chemistry. 55:4639-4642
A reduction-olefination sequence has been used to convert esters to α-fluoro α,β-unsaturated esters. In the presence of diisobutylaluminum hydride, esters are reduced to aldehydes that react in situ with [(EtO) 2 P(O)−CFC(O)OEt] − Li + to form
Autor:
Donald J. Burton, Alagappan Thenappan
Publikováno v:
Journal of Fluorine Chemistry. 48:153-157