Bis -m -phenylene

In the case of NBR-nylon blends it was reported that the addition of the curative m-phenylene-bis-male-imide, improved the strength and stiffness of the blend. An attempt to compare the effect of different curative... 

Chemical Name 5-(2-(tert-Butylamino)-l-hydroxyethyl)-m-phenylene bis(dimethylcarbamate)... 

SYNS DIACETOXYMERCURIPHENOL MERCURY, (4-HYDROXY-m-PHENYLENE)BIS(ACETATO)- PHENOL, 2,4-BIS(ACETOXYMERCURI)-... 

Phenylene)-bis-1H-pyrrole-2,5-dione 1,1 - m-Phenylene)bis-1H-pyrrole-2,5-dione m-Phenyienedimaleimide N,N -m-Phenylenemaleimide NI,N -(m-Phenylenedimaleitnide) N,N -1,3-Phenylenedimaleimide NSC 19639 1H-Pyrrole-2,5-dione, 1,1 -(1,3-phenylene)bis- 1H-Pyrrole-2,5-dione, 1,1 -(phenylene)bis- Vanax MBM. Accelerator free radical regulator and coagent in peroxide-cured polymers. Also used for cross-linking proteins. Solid mp = 197-200 . DuPont UK Vanderbilt R.T. Co. Inc. 

Bis-maleimide as Couplins Asent PP/styrene copolymer blends have been compatibilized by addition of bis-maleimide coupling agent capable of reacting with both polymers. Inoue [1994 a, b] has prepared blends containing 80 parts PP and 20 parts SIS (or SBS) in the presence of 0-0.3 parts m-phenylene bis-maleimide coupling agent on a TSE at 210°C. The blends were characterized by mechanical properties, melt flow rate, DSC, morphology, and selective solvent extraction. Evidence was presented for PP-SIS copolymer formation. 

In earlier studies of the thermolysis and photolysis of m-phenylene-bis(chloro-diazirine) (9) in the presence of 2-vinylpyridine (11) (Scheme 3), it was found that the reaction proceeded in a stepwise fashion, with generation of a monocarbene... 

Yet another synthetic route to obtaining sulfonated FBI involves treatment of the above mentioned polyanion with 4-bromobenzyl sulfonate resulting in poly[2,2 -m-phenylene-bi(N-benzylsulfonate)benzimidazolo-5,5 -diyl] (Scheme 21). 

Very similar, wholly aromatic polyamides, with very regular structures, which reportedly result in better flexibility and higher temperature resistance, were reported. Preparation of these ordered copolyamides can be illustrated as follows. V,V-m-phenylene-bis(m-aminobenzamide) is formed first and then reacted with isophthaloyl chloride by interfacial condensation techniques to yield a product that melts at about 410 C ... 

Methyl-1,3-phenylene) bis (azo)] bis [6-methyl-1,3-benzenediamine] dihydrochloride. See Basic brown 4, dihydrochloride 5,5 -((4-Methyl-1,3-phenylene) bis (azo)) bis (toluene-2,4-diamine). See Basic brown 4 5,S -(4-Methyl-m-phenylene) bis (azo)] bis [toluene-2,4-diamine] dihydrochloride. See Basic brown 4, dihydrochloride 3,3 -(4-Methyl-1,3-phenylene) bis (1,1-dimethyl urea). See Toluene bis (dimethyl urea) 2-Methyl-p-phenylenediamine. See Toluene-2,5-diamine... 

Examples of suitable co-agents are 1,2-polybutadiene, triallyl cyanurate, multiftmc-tional acrylate and methacrylate monomers, and N,hf-m-phenylene-bis(maleimide). 

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