CAS: 31366-25-3; 2,2'-Bi(1,3-Dithiolylidene)

该化合物是一个有机电子捐献器(TTF) , 具有平板, 混合结构, 因其在导电材料和超导材料中的作用而得到广泛承认, 其关键优势在于其可逆的红氧化特性, 能够应用于分子电子学, 有机超导体和电荷转移综合体. TTF 及其衍生物表现出高电子施用能力, 在氧化时形成稳定的基极化, 有利于设计具有可金枪鱼电子特性的功能材料. 该复合体的坚固 --电子系统也使其在有机外效应转晶体(OFETs) 和光伏电装置的合成中具有价值. 它在超分子化学中的多用途进一步凸显了其在先进材料科学和纳米技术应用中的实用性.

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相似化合物

51501-77-0 5058-43-5 51751-16-7

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CAS号255-55-0 1,4-DITHIINO[2,... | CAS号26314-39-6 2,3,6,7-tetrame... | CAS号1863-66-7 1,3-dithiol-1-i... | CAS号57223-41-3 4-bromotetrathi... | CAS号1072505-69-1 (Si2Me4)(TTF)2 | CAS号1072505-60-2 TTF(SiMe2H) | CAS号1072505-66-8 TTF(Si2Me5) | CAS号930-35-8 1,3-二硫酸-2-硫酮 | CAS号40210-84-2 四硫富瓦烯-7,7,8,8-四... | CAS号141858-23-3 bis[2-(1,3-dith... | CAS号51501-77-0 四(甲硫代)四硫富瓦烯 | CAS号66946-48-3 双(乙撑二硫)四硫富瓦烯 | CAS号66946-49-4 双(三亚甲基二硫代)四硫富瓦烯 | CAS号128881-69-6 2-(1,3-dithiol-... | CAS号128881-57-2 1-[2-(1,3-dithi... | CAS号128881-70-9 2-(1,3-dithiol-... | CAS号118148-28-0 2-(1,3-dithiol-... | CAS号137552-55-7 tris[2-(1,3-dit...

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    专利信息


    专利号:US-6603070-B2
    优先权日:2000-07-21
    标题 :Convergent synthesis of multiporphyrin light-harvesting rods
    发明人:LINDSEY JONATHAN S; LOEWE ROBERT S
    权利人:UNIV NORTH CAROLINA STATE
    摘要:The present invention provides a convergent method for the synthesis of light harvesting rods. The rods are oligomers of the formula A 1 (A b+1 ) b , wherein b is at least 1, A 1 through A b+1 are covalently coupled rod segments, and each rod segment A 1 through A 1+b comprises a compound of the formula X 1 (X m+1 ) m wherein m is at least 1 and X 1 through X m+1 are covalently coupled porphyrinic macrocycles. Light harvesting arrays and solar cells containing such light harvesting rods are also described, along with intermediates useful in such methods and rods produced by such methods.

    专利号:WO-0132645-A1
    优先权日:1999-11-04
    标题:The synthesis of extended bis(ethylenedithio)tetrathiafulvalene derivatives and their dihydroxyl analogues
    发明人:OZTURK TURAN; TURKSOY FIGEN; WALLIS JOHN D; UMIT TUNCA
    权利人:TUBITAK MARMARA RES CT; OZTURK TURAN; TURKSOY FIGEN; WALLIS JOHN D; UMIT TUNCA
    摘要:The present invention describes the synthesis of six novel derivatives of bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF), utilising the recently developed reaction of 1,8-diketones with Lawesson's reagent. These new BEDT-TTF derivatives (1)-(6) have potential to delocalise the positive charges formed during change-transfer salts to the peripheral. In addition to their positive charge delocalisation feature, the compounds (1)-(3) have the potential of being introduced hydrogen bonding groups and the compound (4)-(6) already have hydrogen bonding hydroxyl groups. All the new BEDT-TTF (7) derivatives described in this invention have shown comparative CV measurements with the BEDT-TTF. Each of these bis(ethylenedithio)tetrathiafulvalene derivatives of the present invention has a unique and novel structure which can not be found in the prior art and is useful for the development of new organic charge-transfer complexes.

    专利号:US-6916982-B2
    优先权日:2000-07-21
    标题:Synthesis of perylene-porphyrin building blocks and polymers thereof for the production of light-harvesting arrays
    发明人:LOEWE ROBERT S; TOMIZAKI KIN-YA; LINDSEY JONATHAN S
    权利人:UNIV NORTH CAROLINA STATE
    摘要:The present invention provides methods, compounds, and compositions for the synthesis of light harvesting arrays, such arrays comprising: (a) a first substrate comprising a first electrode; and (b) a layer of light harvesting rods electrically coupled to said first electrode, each of said light harvesting rods comprising a polymer of Formula I:n nX 1 X m+1 ) m   (I)n nwherein m is at least 1; X 1 is a charge separation group, and X 2 through X m+1 are chromophores. At least one of X 2 through X m+1 has at least one perylene group coupled thereto.

    专利号:WO-0031302-A1
    优先权日:1998-11-25
    标 题:In situ binary synthesis of biologically effective molecules
    发明人:ECKER DAVID J
    权利人:ISIS PHARMACEUTICALS INC; ECKER DAVID J
    摘要:A plurality of oligonucleotides are caused to bind specifically to target nucleic acid which is predictive of a disease state or a biological condition within cells containing the target nucleic acid. The respective oligonucleotides, which may be functionilized or may be present in the form of oligonucleotide analogs, carry with them a plurality of synthons. Such synthons, which may be identiphores, toxiphores, or other precursors to biologically effective molecules, interact when specific binding of the respective oligonucleotides occurs at sites adjacent to each other on the target nucleic acid. The resulting interaction gives rise to the synthesis, generation or release of highly active biological molecules in situ in the cell in which the specific binding takes place. This permits the use of extraordinarily toxic molecules for use in killing cells containing the target nucleic acids. Imaging and other uses are also provided by the present invention.

    专利号:US-6492111-B1
    优先权日:1998-11-25
    标题 :In situ binary synthesis of biologically effective molecules
    发明人:ECKER DAVID J
    权利人:ISIS PHARMACEUTICALS INC
    摘要:A plurality of oligonucleotides are caused to bind specifically to target nucleic acid which is predictive of a disease state or a biological condition within cells containing the target nucleic acid. The respective oligonucleotides, which may be functionilized or may be present in the form of oligonucleotide analogs, carry with them a plurality of synthons. Such synthons, which may be identiphores, toxiphores, or other precursors to biologically effective molecules, interact when specific binding of the respective oligonucleotides occurs at sites adjacent to each other on the target nucleic acid. The resulting interaction gives rise to the synthesis, generation or release of highly active biological molecules in situ in the cell in which the specific binding takes place. This permits the use of extraordinarily toxic molecules for use in killing cells containing the target nucleic acids. Imaging and other uses are also provided by the present invention.

    专利号:US-4465845-A
    优先权日:1982-04-26
    标题:High pressure synthesis of sulfur-selenium fulvalenes
    发明人:OKAMOTO YOSHIYUKI; WOJCIECHOWSKI PIOTR S
    权利人:KOPPERS CO INC
    摘要:A process is disclosed for one-step preparation of sulfur-selenium fulvalenes by reaction of an acetylenic compound with carbon selenide sulfide or with a mixture of carbon diselenide and carbon disulfide under pressures of at least about 1,000 atmospheres. Fulvalene compounds made by the process are characterized in having at least one sulfur atom and at least one selenium atom in the ring structure of the fulvalene compound. Substituted diselenadithiafulvalenes made by this process are precursors to very pure diselenadithiafulvalene which is useful in preparing charge-transfer salts.

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    主要参考文献

    [参考文献]: Alan C Luntz, Et Al. Nonaqueous Li-Air Batteries: A Status Report. Chem Rev. 2014 Dec 10;114(23):11721-50.
    [参考文献]: Ayca Erdem, Et Al. The Short-Term Toxic Effects Of Tionanoparticles Toward Bacteria Through Viability, Cellular Respiration, And Lipid Peroxidation. Environ Sci Pollut Res Int. 2015 Nov;22(22):17917-24.
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    [参考文献]: Jianli Chen, Et Al. Cisplatin Resistance In Human Cervical, Ovarian And Lung Cancer Cells. Cancer Chemother Pharmacol. 2015 Jun;75(6):1217-27.
    [参考文献]: Kent A Nielsen, Et Al. Self-Assembly Of Dimeric Tetrathiafulvalene-Calix[4]Pyrrole: Receptor For 1,3,5-Trinitrobenzene. Org Lett. 2011 Dec 2;13(23):6176-9.

    合成参考文献


    参考文献:10.1021/ja910721s
    摘要:Wang C, Chen Q, Sun F, Zhang D, Zhang G, Huang Y, Zhao R, Zhu D. Multistimuli responsive organogels based on a new gelator featuring tetrathiafulvalene and azobenzene groups: reversible tuning of the gel-sol transition by redox reactions and light irradiation. J Am Chem Soc. 2010 Mar 10;132(9):3092–6. doi: 10.1021/ja910721s.
    参考文献:10.1002/chem.200500934
    摘要:Choi JW, Flood AH, Steuerman DW, Nygaard S, Braunschweig AB, Moonen NN, Laursen BW, Luo Y, DeIonno E, Peters AJ, Jeppesen JO, Xu K, Stoddart JF, Heath JR. Ground-state equilibrium thermodynamics and switching kinetics of bistable [2]rotaxanes switched in solution, polymer gels, and molecular electronic devices. Chemistry. 2005 Dec 16;12(1):261–79. doi: 10.1002/chem.200500934.
    参考文献:10.1107/s1600536811018800
    摘要:Li H, Wang G, Xiao X. 4-(2-Cyano-ethyl-sulfan-yl)-5'-(pyridin-4-yl)tetra-thia-fulvalene. Acta Crystallogr Sect E Struct Rep Online. 2011 Jun 01;67(Pt 6):o1467.
    参考文献:10.1063/1.3600066
    摘要:Kato T. New method of accurate estimation of the electron-phonon coupling constants in fractionally charged incommensurate electronic states in molecular systems. J Chem Phys. 2011 Jul 14;135(2):024103. doi: 10.1063/1.3600066.
    参考文献:10.1107/s0108768111024608
    摘要:Bruno IJ, Shields GP, Taylor R. Deducing chemical structure from crystallographically determined atomic coordinates. Acta Crystallogr B Struct Sci. 2011 Jul 18;67(4):333–49. doi: 10.1107/s0108768111024608.
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