CAS: 1499-10-1; 9,10-Diphenylanthracene

该化合物其结构特征为:由9和10个位置上的两个联苯组组成的炭疽岩芯,9,10-二苯乙烯(DPA),以其强大的荧光特性著称的多环芳烃(PAH),在包括有机光排放二极管(OLEDs)在内的各种应用中以及作为光物理研究中的荧光探测器,都有用; DEA通常是在室内温度下的固体,在水中呈现高熔点和低溶解度,但在苯和甲苯等有机溶剂中是可溶性的,其分子结构有助于其稳定性和进行光化学反应的能力; 此外,9,10-二苯乙烯因其在有机光伏打中的潜在作用以及由于在引光下有效光排放而作为辐射探测的焚化材料,已经进行了研究. 然而,与许多PAHAH一样,它可能对环境和健康构成风险,需要谨慎处理和处置.

结构式图片

相似化合物

43217-31-8 625854-02-6 201731-79-5

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

CAS号6318-17-8 9,10-Anthracene... | CAS号523-27-3 9,10-二溴蒽 | CAS号98-80-6 苯硼酸 | CAS号605-48-1 9,10-二氯蒽 | CAS号100-58-3 苯基溴化镁 | CAS号108-86-1 溴苯 | CAS号19061-38-2 9,10-dihydro-9,... | CAS号73475-39-5 2-(trifluoromet... | CAS号15257-17-7 9,10-Epidioxyan... | CAS号2026-21-3 1-(9,10-dipheny... | CAS号781-43-1 9,10-二甲基蒽 | CAS号15257-17-7 9,10-Epidioxyan... | CAS号1499-10-1 9,10-二苯基蒽 | CAS号2154-56-5 癸酸苄酯 | CAS号2348-55-2 s-butyl radical | CAS号2492-36-6 n-butyl (radical) | CAS号3744-21-6 2,2-dimethylpropane

合成工艺路线路线简述

    9,10-二溴蒽置于ni(Dppe)Cl2体系中,用 四氢呋喃 用作溶剂,以81.7%的收率获得9,10-二联苯蒽
    参考文献:Process For Producing 9,10-Diphenylanthracene
    标题:Process For Producing 9,10-Diphenylanthracene
    摘要:9,10-二苯基蒽是一种可以通过将9,10-二卤代蒽和金属或半金属苯基化合物进行交叉偶联反应而在一个或两个工艺步骤中适用于工业用途的产物.

    海关参考信息

    专利信息


    专利号:US-2021323987-A1
    优先权日:2018-08-20
    标题:Methods for the Synthesis of Heteroatom Containing Polycyclic Aromatic Hydrocarbons
    发明人:GARG NEIL K; DARZI EVAN R; BARBER JOYANN S; SUSICK ROBERT; CHARI JASON; SPENCE KATIE
    权利人:UNIV CALIFORNIA
    摘要:Methods for the synthesis of polycyclic aromatic hydrocarbons and synthesis platforms for performing such syntheses are provided. Methods and platforms are provided that allow for the synthesis of aza-polycyclic aromatic hydrocarbons by an expedient ring assembly. Methods and platforms allow for a modular approach to synthesis that provide multiple new C—C bonds in sequential pericyclic reactions, thus giving access to compounds with multiple axes of substitution.

    专利号:US-2023348492-A1
    优先权日:2020-05-04
    标题:Photochemical synthesis of marmycin analogues through a new photochemical reaction involving carbonyl compounds
    发明人:SIVAGURU JAYARAMAN; KANDAPPA SUNIL KUMAR; VALLOLI LAKSHMY KANNADI
    权利人:BOWLING GREEN STATE UNIV
    摘要:Photochemical reactivity of carbonyl compounds leading to the synthesis of the Marmycin core is described. The photochemical reactivity involves an excited state reaction that provides convenient access to bicyclic compounds. The disclosed reactivity is a new photochemical pathway involving 1,3-dicarbonyl compounds and amines as well as for enaminones.

    专利号:US-6417380-B1
    优先权日:1987-12-31
    标 题 :Synthesis of 1,2-dioxetanes and intermediates therefor
    发明人:BRONSTEIN IRENA Y; EDWARDS BROOKS
    摘要:Compounds having the formula: n wherein T is a polycycloalkylidene group (e.g., adamant-2-ylidene); R is a C 1-20 alkyl, aralkyl or cycloalkyl group; and Y is a fluorescent chromophore (e.g., n m-phenylene), produced by reacting a compound having the formula: n with an R-ylating agent (e.g., R 2 SO 4 ) in the presence of an alkali metal alkoxide in a polar aprotic solvent. Also, compounds having the formula: n are produced by reacting a compound having the formula: n with n wherein X is an electronegative leaving group (e.g., a halogen anion such as chloride ion) in the presence of a Lewis base (e.g., a trialkyl-amine) dissolved in an aprotic organic solvent (e.g., benzene or toluene). Also, compounds having the formula n are produced by reacting a compound of the formula n with a tetra-O-acylated-O-hexopyranoside halide, then hydrolyzing off the protective acyl groups. The aforementioned compounds and procedures are useful in the synthesis of enzyme-cleavable 1,2-dioxetane ring systems that can serve as members of a binding pair employed, for example, in chemiluminescent immunoassays, DNA probe assays, and direct assays for an enzyme.

    专利号:US-5777133-A
    优先权日:1987-12-31
    标 题:Synthesis of 1, 2-dioxetanes and intermediates therefor
    发明人:BRONSTEIN IRENA Y; EDWARDS BROOKS
    权利人:TROPIX INC
    摘要:Compounds having the formula: ##STR1## wherein T is a polycycloalkylidene group (e.g., adamant-2-ylidene); R is a C 1-20 alkyl, aralkyl or cycloalkyl group; and Y is a fluorescent chromophore (eg., m-phenylene), produced by reacting a compound having the formula: ##STR2## with an R-ylating agent (e.g., R 2 SO 4 ) in the presence of an alkali metal alkoxide in a polar aprotic solvent. Also, compounds having the formula: ##STR3## are produced by reacting a compound having the formula: ##STR4## wherein X is an electronegative leaving group (e.g., a halogen anion such as chloride ion) in the presence of a Lewis base (e.g., a trialkyl-amine) dissolved in an aprotic organic solvent (e.g., benzene or toluene). Also, compounds having the formula ##STR5## are produced by reacting a compound of the formula ##STR6## with a tetra-O-acylated-O-hexopyranoside halide, then hydrolyzing off the protective acyl groups. The aforementioned compounds and procedures are useful in the synthesis of enzyme-cleavable 1,2-dioxetane ring systems that can serve as members of a binding pair employed, for example, in chemiluminescent immunoassays, DNA probe assays, and direct assays for an enzyme.

    专利号:US-4956477-A
    优先权日:1987-12-31
    标 题:Synthesis of 1,2-dioxetanes
    发明人:BRONSTEIN IRENA Y; EDWARDS BROOKS
    权利人:TROPIX INC
    摘要:Compounds having the formula: ##STR1## wherein T is a polycycloalkylidene group (e.g., adamant-2-ylidene); R is a C 1-20 alkyl, aralkyl or cycloalkyl group; and Y is a fluorescent chromophore (e.g., m-phenylene), produced by reacting a compound having the formula: ##STR2## with an R-ylating agent (e.g., R 2 SO 4 ) in the presence of an alkali metal alkoxide in a polar aprotic solvent. Also, compounds having the formula: ##STR3## are produced by reacting a compound having the formula: ##STR4## wherein X is an electronegative leaving group (e.g., a halogen anion such as chloride ion) in the presence of a Lewis base (e.g., a trialkyl-amine) dissolved in an aprotic organic solvent (e.g., benzene or toluene). Also, compounds having the formula ##STR5## are produced by reacting a compound of the formula ##STR6## with a tetra-O-acylated-O-hexopyranoside halide, then hydrolyzing off the protective acyl groups. The aforementioned compounds and procedures are useful in the synthesis of enzyme-cleavable 1,2-dioxetane ring systems that can serve as members of a binding pair employed, for example, in chemiluminescent immunoassays, DNA probe assays, and direct assays for an enzyme.

    专利号:US-8710220-B2
    优先权日:2009-12-10
    标题 :Synthesis of 8-amino boron dipyrromethenes having blue fluorescence
    发明人:PE A CABRERA EDUARDO; AZAEL CÉSAR FERNANDO; FLORES JUAN ORLANDO
    权利人:PE A CABRERA EDUARDO; AZAEL CÉSAR FERNANDO; FLORES JUAN ORLANDO; UNIV GUANAJUATO
    摘要:A family of six 8-amino boron dipyrromethenes having Formulas 1, 2, 3, 4, 6, and 7 has been prepared. The presence of the amine group alters the emission properties of the boron dipyrromethene, such that these compounds are characterized by unexpected blue fluorescence, providing for potential use as lasers. The compound having formula 1 has very high quantum yield. The 8-amino boron dipyrromethenes are prepared in a straightforward, high yield synthesis by substituting an amine group for the thiomethyl group at the 8 position in 8-thiomethyl boron dipyrromethene. The compounds having Formulas 6 and 7 may be used to incorporate peptides and proteins, thus providing biomolecules marked with fluorescent fragments.
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    主要参考文献

    [参考文献]: C L Catherall, Et Al. Determination Of Absolute Chemiluminescence Quantum Yields For Reactions Of Bis-(Pentachlorophenyl) Oxalate, Hydrogen Peroxide And Fluorescent Compounds. J Biolumin Chemilumin. 1989 Jul-Sep;3(3):147-54.
    [参考文献]: Chenchen Qin, Et Al. Rational Assembly Of A Biointerfaced Core@shell Nanocomplex Towards Selective And Highly Efficient Synergistic Photothermal/photodynamic Therapy. Nanoscale. 2015 Dec 21;7(47):20197-210.
    [参考文献]: David J Vinyard, Et Al. Electrogenerated Chemiluminescence Of 9,10-Diphenylanthracene, Rubrene, And Anthracene In Fluorinated Aromatic Solvents. J Phys Chem A. 2008 Sep 18;112(37):8529-33.
    [参考文献]: J V Arena, Et Al. Regression Analysis Of Electrochemical Data With Expanding Space Grid Digital Simulation At Spherical Electrodes. Anal Chem. 1986 Jun;58(7):1481-8.
    [参考文献]: Jin-Ming Lin, Et Al. Chemiluminescence From The Decomposition Of Peroxymonocarbonate Catalyzed By Gold Nanoparticles. J Phys Chem B. 2008 Jul 3;112(26):7850-5.

    合成参考文献


    摘要:Telmesani, R.; Sun, A. C.; Beeler, A. B.; Stephenson, C. R. J., Science of Synthesis: Flow Chemistry in Organic Synthesis, (2018) 1, 139.
    摘要:Fogel, M. S.; Shellnutt, Z. S.; Koide, K., Science of Synthesis: Dearomatizations, (2026) .
    参考文献:10.1021/ac010128e
    摘要:Maus RG, Wightman RM. Microscopic imaging with electrogenerated chemiluminescence. Anal Chem. 2001 Aug 15;73(16):3993–8. doi: 10.1021/ac010128e.
    参考文献:10.1007/s10895-011-0896-1
    摘要:Li XF, Chi ZG, Xu BJ, Li HY, Zhang XQ, Zhou W, Zhang Y, Liu SW, Xu JR. Synthesis and characterization of triphenylethylene derivatives with aggregation-induced emission characteristics. J Fluoresc. 2011 Sep;21(5):1969–77. doi: 10.1007/s10895-011-0896-1.
    参考文献:10.1038/srep15133
    摘要:Chang W, Zhang M, Zheng S, Li Y, Li X, Li W, Li G, Lin Z, Xie Z, Zhao Z, Lou H. Trapping toxins within lipid droplets is a resistance mechanism in fungi. Scientific Reports. 2015 Oct 14;5(1):15133. doi: 10.1038/srep15133.
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