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2,3-dimethylpentacene | 758706-01-3

中文名称
——
中文别名
——
英文名称
2,3-dimethylpentacene
英文别名
——
2,3-dimethylpentacene化学式
CAS
758706-01-3
化学式
C24H18
mdl
——
分子量
306.407
InChiKey
IYMYRZKGDNUSMK-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    7.6
  • 重原子数:
    24
  • 可旋转键数:
    0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为产物:
    描述:
    1,2-bis(bromomethyl)-4,5-dimethylbenzene 在 lithium aluminium tetrahydride 、 potassium iodide 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 反应 48.0h, 生成 2,3-dimethylpentacene
    参考文献:
    名称:
    Organic Thin Film Transistors Based on 2,3-Dimethylpentacene and 2,3-Dimethyltetracene
    摘要:
    Abstract2,3‐Dimethylpentacene (DMP) and 2,3‐dimethyltetracene (DMT) were synthesized, characterized and employed as the channel material in the fabrication of thin‐film transistors. The two methyl groups increase the chemical stability of the compounds versus the pristine acene analogues. The crystals maintain herringbone‐like molecular packing, whereas the weak dipole associated with the unsymmetrical molecule induces an anti‐parallel alignment among the neighbors. This structural motif favors layered film growth on SiO2/Si surface. Thin film transistors prepared on SiO2/Si and n‐nonyltrichlorosilane‐modified SiO2/Si at different substrate temperatures were compared. DMP‐based transistors prepared on rubbed n‐nonyltrichlorosilane‐modified SiO2/Si substrate gave the highest field‐effect mobility of 0.46 cm2/Vs, whereas DMT‐based transistor gave a mobility of 0.028 cm2/Vs.
    DOI:
    10.1002/jccs.201200383
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同类化合物

并六苯 并五苯 十四氟并五苯 二苯并[去,St]并五苯 二苯并[hi,wx]庚省 二苯并[fg,qr]戊省 二苯并[a,l]并五苯 二苯并[a,c]戊省 7,14-二苯并五苯 6,13-双(三甲硅基乙炔基)并五苯 6,13-双(三异丙基甲硅烷基乙炔基)并五苯 6,13-双(2-噻吩基)并五苯 6,13-二氯并五苯 2,3,9,10-四(4-叔丁基苯基)并五苯 1,4,8,11-戊省四酮,6,13-二己基-2,3,9,10-四甲基- 5-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl]-14-phenylpentacene 5-(4-decyloxy-phenyl)-14-phenyl-pentacene 1,2,3,4,9,10-Hexaphenyl-anthracene 1,4-bis(trimethylsilyl)-2,3-dimethylnaphthacene 6,6’-bipentacene Tri(propan-2-yl)-[2-[7,14,24,31-tetraphenyl-19-[2-tri(propan-2-yl)silylethynyl]-2-nonacyclo[18.14.0.03,18.05,16.06,15.08,13.022,33.023,32.025,30]tetratriaconta-1,3,5(16),6,8,10,12,14,17,19,21,23,25,27,29,31,33-heptadecaenyl]ethynyl]silane Tri(propan-2-yl)-[2-[7,18,28,39-tetraphenyl-23-[2-tri(propan-2-yl)silylethynyl]-2-undecacyclo[22.18.0.03,22.05,20.06,19.08,17.010,15.026,41.027,40.029,38.031,36]dotetraconta-1,3,5(20),6,8,10,12,14,16,18,21,23,25,27,29,31,33,35,37,39,41-henicosaenyl]ethynyl]silane 6,13-bis(triisobutylsilylethynyl)pentacene 1,4-Bis(2,2-dimethylpropoxy)anthracene 2,3-dibromo-6,13-bis(diphenylmethylene)-9,10-bis(dodecyloxy)-6,13-dihydropentacene dimethyl-2,3 diacetoxy-1,4 naphtacene 2,9-didecylpentacene 2,9-diundecylpentacene 2,9-dioctylpentacene 7-Ethyl-heptaphen 2,9-dibutylpentacene 8,9,10-Trichlorocyclohept-s-indacen 2,9-dipentylpentacene 2,3-bis(hexadecyloxy)-5,12-diphenyltetracene naphthacene; compound with antimony (V)-chloride 6,13-bis[4-(trimethylsilylethynyl)phenyl]pentacene 2,8-di(2-(trimethylsilyl)ethylthio)tetracene 2,8-di(acetylthio)tetracene 6,13-bis(cyclopropyldiisopropylsilylethynyl)pentacene naphthacene-5,6-diol 2-(2-(trimethylsilyl)ethylthio)tetracene 6,7,14,15,22,23-Hexamethoxyanthra<2,3-j>heptaphen 2,9-diheptylpentacene 5,14-diphenyl-7,12-bis(2-(triethylsilyl)ethyl)pentacene 5,8-difluorobenzophenanthrene 6,13-bis((1-methylenepropyl)diisopropylsilylethynyl)pentacene