55935-46-1Relevant academic research and scientific papers
LIVING POLYMERIZATION OF METHACRYLIC ESTERS WITH ALUMINIUM PORPHYRIN INITIATORS. AXIAL LIGAND EXCHANGE ACTIVITIES OF ALKYL- AND ENOLATE-ALUMINIUM PORPHYRINS IN RELATION TO THE POLYMERIZATION MECHANISM
Aida, Takuzo,Sugimoto, Hiroshi,Kuroki, Masakatsu,Inoue, Shohei
, p. 249 - 257 (2007/10/02)
Polymerization of methacrylic esters such as benzyl methacrylate using as initiator an-equimolar mixture of methylaluminium 5,10,15,20-tetraphenylporphine and 2,7,12,17-tetramethyl-3,8,13,18-tetramethylporphine proceeded from both initiators, affording a unimodal polymer of narrow molecular weight distribution, although the reactivities of (TPP)AlMe and (EtioP)AlMe are very different from each other. 1H NMR studies on a mixture of two different (porphinato)aluminium enolates, the growing species, and a mixture of a (porphinato)aluminium enolate and an alcoholate, in the absence and presence of methyl methacrylate (MMA or MMA-d8), indicated an acyclic transition state polymerization mechanism by the participation of two aluminium porphyrin molecules, where the growing species always exchange their enolate ligands whenever it grows.
Thermal Degradation of Polymers. I Integrity of Monomer Derived from Thermal Degradation of Poly(methyl methacrylate) and Poly(methacrylonitrile)
Hodder, Anthony N.,Holland, Kelvyn A.,Rae, Ian D.
, p. 1883 - 1887 (2007/10/02)
A random copolymer of methyl methacrylate and its (D5)analogue has been used to show that thermal degradation of the polymer regenerates the original monomer units.A similar results has been obtained for poly(methacrylonitrile).In each case, thermal degradation at 200 deg produced mainly the (D0)- and (D5)-species, while at higher temperatures some (D2)- and (D3)-ions were observed in the mass spectrum of the recovered monomer.
Competing, kc, Borderline, ks, and Carbonyl Addition Processes in Solvolyses of α-Keto Mesylates and Triflates. α-Keto Cations. 5
Creary, Xavier
, p. 5568 - 5577 (2007/10/02)
Solvolysis studies on tertiary α-keto mesylates show quite varying responses in rate to solvent ionizing power.The m values are 1.01 for 2-benzoyl-2-adamantyl mesylate (12), 0.66 for the mesylate derivative of 2-hydroxy-2,4,4-trimethyl-3-pentanone (4), and 0.63 for the mesylate derivative of 2-hydroxy-2-methylpropiophenone (3).The mesylate derivative of methyl α-hydroxyisobutyrate (5) does not correlate well with YOTs values, but instead it gives behavior that parallels that of isopropyl tosylate.Mesylates 3-5 solvolyze giving varying ratios of elimination and substitution products at rates comparable to that of isopropyl mesylate. β-d6 isotope effects for 3 and 4 range from 1.69 to 2.08 and are consistent with the intermediacy of α-keto cations. β-Deuterium isotope effects for 5 are quite variable (1.40-2.52) and parallel the amount of elimination product formed (22-94percent).This is consistent with the intermediacy of a reversibly formed ion-pair intermediate which can suffer proton loss.However, the SN2 (intermediate) mechanism remains a possibility in solvolyses of 5.Mesylate 3 solvolyzed in trifluoroethanol with added triethylamine to give an alkoxyoxirane.With small amounts of added 2,6-lutidine the 1,2-elimination product was major , while with added methanesulfonic acid the rearranged trifluoroethyl ester of dimethylphenyl acetic acid was major.These variable products were interpreted in terms of competing carbonyl addition processes and processes involving the α-keto cation.Secondary triflates derived from α-hydroxypropiophenone, 2,2-dimethyl-4-hydroxy-3-pentanone, and ethyl lactate solvolyzed giving the simple substitution product.Rates parallel solvent nucleophilicity and suggest a ks process involving negligible cationic character at the carbon α to the carbonyl group. kΔ processes are also not involved in solvolyses of these secondary triflates.
