CAS: 630-76-2; Tetraphenylmethane

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CAS号56-23-5 四氯化碳 | CAS号100-59-4 苯基氯化镁 | CAS号76-84-6 三苯基甲醇 | CAS号6303-21-5 次磷酸 | CAS号110-46-3 亚硝酸异戊酯 | CAS号76-83-5 三苯基氯甲烷 | CAS号591-51-5 苯基锂 | CAS号22948-06-7 4-三甲基苯胺 | CAS号1078-58-6 二苯锌 | CAS号105309-59-9 四(4-溴苯)甲烷 | CAS号101-81-5 二苯甲烷 | CAS号519-73-3 三苯基甲烷 | CAS号71-43-2 苯 | CAS号160248-28-2 四(4-羧酸苯基)甲烷 | CAS号3178-23-2 Cyclohexane,1,1... | CAS号828-45-5 Benzene,(1-meth... | CAS号134080-67-4 1-iodo-4-[tris(... | CAS号13619-64-2 Cyclohexyltriph... | CAS号1610-24-8 Cyclohexane,1,1...

合成工艺路线路线简述

    三苯基甲醇置于乙酰氯体系中,用 乙醚,苯 作为反应溶剂,化学反应 4.67H,反应生成 四苯基甲烷
    参考文献:中枢原子尺寸对第十四族四甲苯基甲基扭转的影响
    标题:中枢原子尺寸对第十四族四甲苯基甲基扭转的影响
    摘要:Xiv族四甲苯基系列x(c 6 H 4-Ch 3)4(x = C,Si,Ge,Sn,Pb)是通过使用非弹性中子散射来测量低能声子谱来直接访问甲基扭转模态而研究的.结果表明,分子半径随中心原子大小变化的影响,对甲基动力学具有直接影响,而基于固态结构,分子动力学和接触面计算的发现进一步增强了这种影响.发现最轻的类似物的扭转模式主要是分子内的:Si和ge类似物具有高度的分子间甲基-甲基相互作用,而最重的类似物(sn和pb)在整个声子浴中表现出明显的分子间甲基相互作用.晶格模式.
    DOI:10.1002/chem.201202105

    海关参考信息

    专利信息


    专利号:US-8618281-B2
    优先权日:2006-01-03
    标 题 :Geometric synthesis of porphyrin rods
    发明人:LINDSEY JONATHAN S; YU LIANHE; THAMYONGKIT PATCHANITA; BHISE ANIL D
    权利人:LINDSEY JONATHAN S; YU LIANHE; THAMYONGKIT PATCHANITA; BHISE ANIL D; UNIV NORTH CAROLINA STATE
    摘要:A method of making a compound of Formula I′ n ncomprises reacting a compound of the formula DLCHO, with a compound of the formulan n nto produce the compound of Formula I′. Methods of using the compounds are also described, particularly as intermediates for the synthesis of porphyrin rods, which porphyrin rods are in turn useful for (among other things) the production of molecular memory devices.

    专利号:US-10919904-B2
    优先权日:2016-08-17
    标 题 :Northern-southern route to synthesis of bacteriochlorins
    发明人:LIU YIZHOU; LINDSEY JONATHAN S; ALLU SRINIVASA RAO; FUJITA HIKARU
    权利人:UNIV NORTH CAROLINA STATE
    摘要:Described herein are chlorins, bacteriochlorins, methods and intermediates for the synthesis of bacteriochlorins, and methods of using such bacteriochlorins for, among other things, diagnostic and therapeutic purposes such as luminescent compounds in flow cytometry, and as active agents in photodynamic therapy (PDT).

    专利号:US-11298676-B2
    优先权日:2017-10-17
    标 题:Porous material for storing of molecules and its use
    发明人:DEMEL JAN; HYNEK JAN
    权利人:INST OF INORGANIC CHEMISTRY CAS
    摘要:The invention concerns new types of porous coordination polymers (MOF) and a method for their preparation. MOFs have been prepared through synthesis of salts of trivalent cations M 3+ , the source of which are aluminium, chromium, iron or yttrium salts, it is advantageous if of chlorides, nitrates or sulphates, with linkers carrying two or more phosphinic groups under presence of solvent. Linkers are phenylene-1,4-bis(R phosphinic acid) (PBPA) and biphenylene-4,4′-bis(R phosphinic acid) (BBPA). For the prepared MOFs, the structure has been tested using x-ray powder diffraction, specific surface and porousness which have been characterised through adsorption isotherm of nitrogen and further the stability of prepared MOFs has been determined using thermogravimetric analysis. n All the prepared MOFs have been stable around 400° C. and have contained mesopores or micropores where hydrogen or CO 2 , for example, can be stored.

    专利号:US-4565896-A
    优先权日:1984-10-22
    标 题 :Process for low pressure synthesis of ethylene glycol from synthesis gas
    发明人:KNIFTON JOHN F; DURANLEAU ROGER G
    权利人:TEXACO INC
    摘要:This invention relates to the manufacture of ethylene glcyol and more particularly to a low pressure process for making ethylene glycol comprising reacting synthesis gas, i.e. a mixture of carbon monoxide and hydrogen, plus formaldehyde in the presence of a homogeneous liquid catalyst containing an effective amount of cobalt-containing compound and a silicon or germanium-containing promoter and a solvent at a temperature of at least 50 DEG C. and a pressure of at least 500 psi wherein said ethylene glycol product separates as a separate liquid phase from the solvent.

    专利号:US-4568780-A
    优先权日:1984-10-22
    标 题 :Process for low pressure synthesis of ethylene glycol from synthesis gas plus 1,3-dioxolane
    发明人:KNIFTON JOHN F
    权利人:TEXACO INC
    摘要:This invention relates to the manufacture of ethylene glycol and more particularly to a low pressure process for making ethylene glycol comprising reacting synthesis gas, i.e. a mixture of carbon monoxide and hydrogen, plus 1,3-dioxolane in the presence of a homogenous liquid catalyst containing an effective amount of cobalt-containing compound and a silane or germane-containing promoter dispersed in a hydrocarbon solvent at a temperature of at least 50 DEG C. and a pressure of at least 500 psi, where the particular solvents used allow the desired product to be separated from the reaction mixture by phase separation.

    专利号:US-10968308-B2
    优先权日:2017-11-07
    标 题 :Preparation method of epoxy compound having alkoxysilyl group, epoxy compound having alkoxysilyl group, composition comprising the same, and use thereof
    发明人:CHUN HYUN AEE; KIM YUN JU; PARK SOOK YEON; PARK SU JIN
    权利人:KOREA INST IND TECH
    摘要:Provided are a preparation method of an epoxy compound having an alkoxysilyl group in which an increase in the epoxy equivalent weight (EEW) of the epoxy compound is minimized because alkoxysilylation occurs through a simple one-step reaction using a hydroxyl group formed during the synthesis of the epoxy compound, an epoxy compound having an alkoxysilyl group prepared by the method, a composition comprising the same, and a use thereof. The method includes the reaction of an epoxy compound having a hydroxyl group with an isocyanate alkoxysilane in the presence of amine-based base catalyst, wherein the epoxy compound having an alkoxysilyl group has a mole ratio of [epoxide group]:[alkoxysilyl group] of n:1 ranging from 2:1 to 10:1, and an EEW increase of the epoxy compound having an alkoxysilyl group is less than 260/n. The epoxy compound has good physical properties when being cured.
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    合成参考文献


    摘要:Mark, I. E., Science of Synthesis, (2004) 7, 458.
    摘要:Mark, I. E., Science of Synthesis, (2004) 7, 459.
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