Catalytic conversion of amide compounds to methyl ether polymers and methyl ether ladder polymers
    56.
    发明申请
    Catalytic conversion of amide compounds to methyl ether polymers and methyl ether ladder polymers 审中-公开
    酰胺化合物催化转化成甲基醚聚合物和甲基醚梯度聚合物

    公开(公告)号:US20100168377A1

    公开(公告)日:2010-07-01

    申请号:US12317796

    申请日:2008-12-29

    IPC分类号: C08G73/00

    摘要: Catalytic processes have been developed for direct chemical conversion of amides to methyl ether polymers or methyl ether ladder polymers. Amides formed by reacting acetic acid with monoethanol amine (MEA) or acetic acid with butylamine were polymerized in the presence of transition metal catalysts in air to form linear polymers. Ethanol acetamide was catalytically converted to a linear polyether as characterized by FTIR spectra. The catalysts were based on molecular strings of mono-, di- or tri-valent transition metal compounds that opened the amide carbonyl double bond to produce linear polyethers. Laboratory results have demonstrated [cobalt(II)]2, [manganese(II)]2, cobalt(II)-manganese(II), [nickel(II)]2 and related families of catalysts to be effective for formation of methyl ether polymers by this process.Similar transition metal catalysts plus hydrogen peroxide facilitated reactions of the amide compounds dimethylacetamide (DMAc), DMF as well as amides formed from L-cysteine with MEA, serine with MEA, arginine with MEA and histidine with MEA to form insoluble methyl ether ladder polymers at or near ambient temperature that were quite different from the linear polyether polymers. Catalysts active for these polymerizations were based on di- or tri-valent transition metals. The polymer formed from DMAc using a Co(III) catalyst plus 20% hydrogen peroxide was a ladder polymer as characterized by FTIR spectroscopy and isolated solids were observed to be microscopic hexagonal needle shaped crystals. The catalysts were based on molecular strings of tri-valent transition metal compounds. Laboratory results have demonstrated [cobalt(III)]2 and related families of catalysts in the presence of hydrogen peroxide to be effective for formation of methyl ether ladder polymers.

    摘要翻译: 已经开发了用于将酰胺直接化学转化为甲基醚聚合物或甲基醚梯度聚合物的催化方法。 在乙酸与单乙醇胺(MEA)或乙酸与丁胺反应形成的酰胺在空气中在过渡金属催化剂存在下聚合形成线性聚合物。 将乙醇乙酰胺催化转化为线性聚醚,其特征在于FTIR光谱。 催化剂基于打开酰胺羰基双键以产生线性聚醚的单 - ,二 - 或三价过渡金属化合物的分子串。 实验室研究结果表明[钴(Ⅱ)] 2,[锰(Ⅱ)] 2,钴(Ⅱ) - 锰(Ⅱ),[镍(Ⅱ) 聚合物通过这个过程。 类似的过渡金属催化剂加过氧化氢促进了酰胺化合物二甲基乙酰胺(DMAc),DMF以及由L-半胱氨酸与MEA形成的酰胺,具有MEA的丝氨酸,具有MEA的精氨酸和具有MEA的组氨酸形成不溶性甲基醚梯度聚合物的酰胺化合物 或接近环境温度,与线性聚醚聚合物完全不同。 对这些聚合有活性的催化剂基于二价或三价过渡金属。 使用Co(III)催化剂和20%过氧化氢由DMAc形成的聚合物是通过FTIR光谱表征的梯形聚合物,并且观察到分离的固体是微观六角形针状晶体。 催化剂基于三价过渡金属化合物的分子串。 实验室结果表明,在过氧化氢存在下,[钴(III)] 2和催化剂的相关族可有效形成甲基醚梯形聚合物。

    Polymers of 2-ketopentafluoropropanesulfonic acid and related acids with
ethylene or fluorinated unsaturated monomers
    58.
    发明授权
    Polymers of 2-ketopentafluoropropanesulfonic acid and related acids with ethylene or fluorinated unsaturated monomers 失效
    2-酮戊基丙磺酸和相关酸与乙烯或氟化不饱和单体的聚合物

    公开(公告)号:US4214070A

    公开(公告)日:1980-07-22

    申请号:US4482

    申请日:1979-01-18

    申请人: Carl G. Krespan

    发明人: Carl G. Krespan

    摘要: 2-Ketopentafluoropropanesulfonic acid is obtained as a product of the reaction of sulfur trioxide and ethyl pentafluoroisopropenyl ether or by transesterification from corresponding esters. Similar sulfonic acids may be obtained by the latter process. The new compounds are useful as monomers for producing polymers, particularly moldable, dyeable, fluoropolymers, and as cationic initiators, e.g., for tetrahydrofuran polymerization.

    摘要翻译: 作为三氧化硫和五氟异丙烯基乙酯的反应的产物或通过相应的酯的酯交换得到2-酮戊基丙磺酸。 可以通过后一种方法获得类似的磺酸。 新化合物可用作生产聚合物的单体,特别是可成型的,可染色的,含氟聚合物,以及阳离子引发剂,例如四氢呋喃聚合。

    Prepolymer dianhydrides
    59.
    发明授权
    Prepolymer dianhydrides 失效
    预聚物二酐

    公开(公告)号:US4196129A

    公开(公告)日:1980-04-01

    申请号:US933186

    申请日:1978-08-14

    CPC分类号: C07D493/14 C08G67/00

    摘要: A process for preparing dianhydrides that are miscible with hydroxyl prepolymers at moderate temperatures and can cure hydroxyl prepolymers to elastomers at moderate temperatures is disclosed. The dianhydrides are prepared by solution reaction of a prepolymer diol with excess dianhydride followed by removal of unreacted dianhydride. The prepolymer dianhydrides are miscible with hydroxyl substituted hydrocarbon prepolymers and cure the prepolymers to polyester-linked elastomers.

    摘要翻译: 公开了一种制备在中等温度下可与羟基预聚物混溶并可在中等温度下将羟基预聚物固化至弹性体的二酐的方法。 二酐通过预聚物二醇与过量二酐的溶液反应制备,然后除去未反应的二酐。 预聚物二酐与羟基取代的烃预聚物可混溶,并将预聚物固化成聚酯连接的弹性体。