CAS: 867044-28-8; (9,10-Di(Naphthalen-2-yl)Anthracen-2-yl)Boronic Acid

该化合物是一种有机化合物,其特点是结构复杂,包括一个炭疽芯,替换成两个2-纳弗基组和一个碳酸功能组,该化合物通常具有很强的荧光作用,因此对有机电子和光度应用感兴趣;存在碳酸碱可与二醇发生潜在互动,可用于各种化学反应,包括铃木组合反应,增强其在合成有机化学中的效用;此外,该化合物的结构有助于其稳定性和溶解性,这对于材料科学的应用至关重要;其分子设计还可能具有特定的电子特性,从而有可能用于有机发光二极(OLEDs)和其他光电子设备;

结构式图片

相似化合物

597553-98-5 872050-52-7 400607-47-8

上下游产品

CAS号474688-76-1 2-溴-9,10-双(2-萘基)蒽 | CAS号121-43-7 硼酸三甲酯 | CAS号5419-55-6 硼酸三异丙酯

合成工艺路线路线简述

  • 62394-19-8 + 572-83-8 = 867044-28-8
    反应条件:1.1 Solvents: Tetrahydrofuran; -20 °C; 1 H,-20 °C; -20 °C -> Rt; Rt1.2 Reagents: Water; 1 H,Cooled2.1 Reagents: Potassium Iodide,Sodium Hypophosphite Solvents: Acetic Acid; 4 H,100 °C3.1 Reagents: Tert-Butyllithium Solvents: Tetrahydrofuran; -78 °C; 1 H,-78 °C3.2 Reagents: Triisopropyl Borate; -78 °C; 1 H,-78 °C; -78 °C -> Rt3.3 Reagents: Hydrochloric Acid Solvents: Water; 1 H,Rt
    标题:Synthesis Of 9,10-Di(β-Naphthyl)Anthracene-2-Boronic Acid
    作者:Zhu,Yan-Long; Et Al
    参考文献:Huaxue Shiji 日期:2014 卷标:36(8) 页码:693-695]

    474688-76-1 = 867044-28-8
    反应条件:1.1 Reagents: Tert-Butyllithium Solvents: Tetrahydrofuran; -78 °C; 1 H,-78 °C1.2 Reagents: Triisopropyl Borate; -78 °C; 1 H,-78 °C; -78 °C -> Rt1.3 Reagents: Hydrochloric Acid Solvents: Water; 1 H,Rt
    标题:Synthesis Of 9,10-Di(β-Naphthyl)Anthracene-2-Boronic Acid
    作者:Zhu,Yan-Long; Et Al
    参考文献:Huaxue Shiji 日期:2014 卷标:36(8) 页码:693-695]

    = 867044-28-8
    反应条件:1.1 Reagents: Triisopropyl Borate Solvents: Tetrahydrofuran; -78 °C; 1 H,-78 °C; -78 °C -> Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; 1 H,Rt
    标题:Synthesis Of 9,10-Di(β-Naphthyl)Anthracene-2-Boronic Acid
    作者:Zhu,Yan-Long; Et Al
    参考文献:Huaxue Shiji 日期:2014 卷标:36(8) 页码:693-695]

    474688-75-0 = 867044-28-8
    反应条件:1.1 Reagents: Potassium Iodide,Sodium Hypophosphite Solvents: Acetic Acid; 4 H,100 °C2.1 Reagents: Tert-Butyllithium Solvents: Tetrahydrofuran; -78 °C; 1 H,-78 °C2.2 Reagents: Triisopropyl Borate; -78 °C; 1 H,-78 °C; -78 °C -> Rt2.3 Reagents: Hydrochloric Acid Solvents: Water; 1 H,Rt
    标题:Synthesis Of 9,10-Di(β-Naphthyl)Anthracene-2-Boronic Acid
    作者:Zhu,Yan-Long; Et Al
    参考文献:Huaxue Shiji 日期:2014 卷标:36(8) 页码:693-695]

    7321-27-9 + 572-83-8 = 867044-28-8
    反应条件:1.1 Reagents: Butyllithium Solvents: Tetrahydrofuran; -20 °C; 1 H,-20 °C1.2 Solvents: Tetrahydrofuran; -20 °C; 1 H,-20 °C; -20 °C -> Rt1.3 Reagents: Water; 1 H,Cooled1.4 Reagents: Potassium Iodide,Sodium Hypophosphite Solvents: Acetic Acid; 4 H,100 °C2.1 Reagents: Tert-Butyllithium Solvents: Tetrahydrofuran; -78 °C; 1 H,-78 °C2.2 Reagents: Triisopropyl Borate; -78 °C; 1 H,-78 °C; -78 °C -> Rt2.3 Reagents: Hydrochloric Acid Solvents: Water; 1 H,Rt
    标题:Synthesis Of 9,10-Di(β-Naphthyl)Anthracene-2-Boronic Acid
    作者:Zhu,Yan-Long; Et Al
    参考文献:Huaxue Shiji 日期:2014 卷标:36(8) 页码:693-695]

    7321-27-9 = 867044-28-8
    反应条件:1.1 Reagents: Butyllithium Solvents: Tetrahydrofuran; -20 °C; 1 H,-20 °C2.1 Solvents: Tetrahydrofuran; -20 °C; 1 H,-20 °C; -20 °C -> Rt; Rt2.2 Reagents: Water; 1 H,Cooled3.1 Reagents: Potassium Iodide,Sodium Hypophosphite Solvents: Acetic Acid; 4 H,100 °C4.1 Reagents: Tert-Butyllithium Solvents: Tetrahydrofuran; -78 °C; 1 H,-78 °C4.2 Reagents: Triisopropyl Borate; -78 °C; 1 H,-78 °C; -78 °C -> Rt4.3 Reagents: Hydrochloric Acid Solvents: Water; 1 H,Rt
    标题:Synthesis Of 9,10-Di(β-Naphthyl)Anthracene-2-Boronic Acid
    作者:Zhu,Yan-Long; Et Al
    参考文献:Huaxue Shiji 日期:2014 卷标:36(8) 页码:693-695
📜2-溴-9,10-双(2-萘基)蒽置于盐酸,正丁基锂体系中,用 四氢呋喃,正己烷 作为反应溶剂,化学反应生成 9,10-双(2-萘基)蒽-2-硼酸
参考文献:Semiconducting Material Comprising Aza-Substituted Phosphine Oxide Matrix And Metal Salt
标题:Semiconducting Material Comprising Aza-Substituted Phosphine Oxide Matrix And Metal Salt
摘要:本发明涉及一种半导体材料,其中包括至少一种金属阳离子和一种氮代磷氧化物化合物的盐或络合物,具有改进的电学性能,以及适用于该有机半导体材料的化合物和利用该半导体材料的改进电学性能的电子器件.

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