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Preparing isobutene polymer, useful e.g. as fuel additives, comprises polymerizing isobutene/isobutene containing monomeric mixture in the presence of Lewis acid, initiators and a compound e.g. orthocarbonic acid ester
Preparing isobutene polymer, useful e.g. as fuel additives, comprises polymerizing isobutene/isobutene containing monomeric mixture in the presence of Lewis acid, initiators and a compound e.g. orthocarbonic acid ester
Preparing isobutene polymer comprises polymerizing isobutene or isobutene containing monomeric mixture in the presence of Lewis acid, initiators and at least compound (A) from a metal containing compound; orthocarbonic acid ester (c) and/or an epoxy compound (d). Preparing isobutene polymer comprises polymerizing isobutene or isobutene containing monomeric mixture in the presence of Lewis acid, initiators and at least compound (A) from a metal containing compound of formula (MZ m(OR 1) n) (a), (MZ o(OR 2) p) (b) or (MZ q(OR 1) r) (a1); orthocarbonic acid ester of formula (R 7-C(OR 8) 3) (c) and/or an epoxy compound of formula (d). M : metal or metalloid, preferably B, Al, Si, Sn(IV), Ti(IV), V or Fe(III); Z, Y 1halo; R 11-6C alkyl; R 2CR 3R 4-CY 1R 5R 6; R 3-R 6H, 1-10C alkyl or aryl; R 7H, 1-4C alkyl or phenyl; R 81-6C alkyl; R 9, R 10H or 1-10C alkyl; m, o : 0-4; n, p : 1-5; and either q, r : 0-4; or q+r : an oxidation number of M. Where: the sum of m and n corresponds to the oxidation number of M. Independent claims are included for: (1) an isobutene polymer obtained by the process; and (2) a process for functionalizing the isobutene-polymer by hydrosilylation-, hydrosulfonation-, electrophilic aromatic substitution-, epoxidation- process and optionally reacting with a nucleophile, or hydroboration and optionally oxidative separation process, or converting with an enophile in an En-reaction, or addition of halo and halo-hydro compound, or hydroformylation and optionally hydrogenation process, or reductive amination process, or copolymerization with an olefinic unsaturated dicarboxylic acid or its derivative, or amination of nucleophilic substitution. [Image].
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机译:制备异丁烯聚合物包括在路易斯酸,引发剂和至少一种化合物(A)的存在下,从一种含金属的化合物聚合异丁烯或含异丁烯的单体混合物。原碳酸酯(c)和/或环氧化合物(d)。制备异丁烯聚合物包括在路易斯酸,引发剂和至少一种化合物(A)的存在下,由含金属的式(MZ m(OR 1>)n)(a),(MZ o)的化合物聚合异丁烯或含异丁烯的单体混合物。 (OR 2>)p)(b)或(MZ q(OR 1>)r)(a1);式(R 7> -C(OR 8>)3)(c)的原碳酸酯和/或式(d)的环氧化合物。 M:金属或准金属,优选B,Al,Si,Sn(IV),Ti(IV),V或Fe(III); Z,Y 1> halo; R 1> 1-6C烷基; R 2> CR 3> R 4> -CY 1> R 5> R 6>; R 3> -R 6> H,1-10C烷基或芳基; R 7> H,1-4C烷基或苯基; R 8> 1-6C烷基; R 9>,R 10> H或1-10C的烷基; m,o:0-4; n,p:1-5;和q,r:0-4;其中,m和n之和对应于M的氧化数。(1)通过该方法制得的异丁烯聚合物;或q + r:M的氧化数。 (2)通过氢化硅烷化,加氢磺化,亲电芳族取代,环氧化过程和任选地与亲核试剂反应,或氢硼化和任选地氧化分离过程或与亲烯转化为En来官能化异丁烯聚合物的方法-反应,或添加卤代和卤代氢化合物,或加氢甲酰化和任选地加氢的方法,或还原性胺化的方法,或与烯属不饱和二羧酸或其衍生物的共聚,或亲核取代的胺化。 [图片]。
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