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dimethyl (1α,4α,4aβ,4bα,4cβ,5α,10α,10aβ,10bα,10cβ)-1,4,4a,4b,4c,5,10,10a,10b,10c-decahydro-1,4:5,10-dimethano-6,9-dimethoxybenzo<3',4'>cyclobuta<1',2':3,4>cyclobuta<1,2-b>naphthalene-4b,10b-dicarboxylate | 124639-14-1

中文名称
——
中文别名
——
英文名称
dimethyl (1α,4α,4aβ,4bα,4cβ,5α,10α,10aβ,10bα,10cβ)-1,4,4a,4b,4c,5,10,10a,10b,10c-decahydro-1,4:5,10-dimethano-6,9-dimethoxybenzo<3',4'>cyclobuta<1',2':3,4>cyclobuta<1,2-b>naphthalene-4b,10b-dicarboxylate
英文别名
dimethyl-(1α,4α,4aβ,4bα,4cβ,5α,10α,10aβ,10bα,10cβ)-1,4,4a,4b,4c,5,10,10a,10b,10c-decahydro-6,9-dimethoxy-1,4:5,10-dimethanobenzo<3',4'>cyclobuta<1',2':3,4>cyclobuta<1,2-b>naphthalene-4b,10b-dicarboxylate;dimethyl (1α,4α,4aβ,4bα,4cβ,5α,10α,10aβ,10bα,10cβ)-6,9-dimethoxy-1,4,4a,4c,5,10,10a,10c-octahydro-1,4:5,10-dimethanobenzo<3',4'>cyclobuta<1',2':3,4>cyclobuta<1,2b>naphthalene-4b,10b-dicarboxylate;dimethyl (1α,4α,4aβ,4bα,4cβ,5α,10α,10aβ,10bα,10cβ)-6,9-dimethoxy-1,4,4a,4c,5,10,10a,10c-octahydro-1,4:5,10-dimethanobenzo[3',4']cyclobuta[1',2':3,4]cyclobuta[1,2b]naphthalene-4b,10b-dicarboxylate
dimethyl (1α,4α,4aβ,4bα,4cβ,5α,10α,10aβ,10bα,10cβ)-1,4,4a,4b,4c,5,10,10a,10b,10c-decahydro-1,4:5,10-dimethano-6,9-dimethoxybenzo<3',4'>cyclobuta<1',2':3,4>cyclobuta<1,2-b>naphthalene-4b,10b-dicarboxylate化学式
CAS
124639-14-1
化学式
C26H28O6
mdl
——
分子量
436.505
InChiKey
XIIVATMPKLBOSV-IEEIZPPOSA-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):
    3.31
  • 重原子数:
    32.0
  • 可旋转键数:
    4.0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    71.06
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis of a Variety of Bichromophoric “Ball-and-Chain” Systems Based on Buckminsterfullerene (C60) for the Study of Intramolecular Electron and Energy Transfer Processes
    摘要:
    Diels-Alder reaction of C-60 with the 1,3-dienes 7e-h, 8a, 8b, and 8d-h affords the ''ball-and-chain'' systems 2e-h, 3a, 3b, and 3d-h bearing two chromophores linked via a rigid, hybrid saturated polynorbornane-bicyclo[2.2.0]hexane (''norbornylogous'') hydrocarbon bridge. Analogous reaction with the bis(diene) 9 affords the soluble dumbbell system 4 bearing two C-60, chromophores. The norbornylogous bridge is a strong mediator of electron and energy transfer via a through-bond coupling mechanism. The norbornylogous donor-bridge-diene units 7d-h, 8a, 8b, and 8d-h were prepared in a straightforward manner from bicyclo[2.2.2]octane precursors by extending the bridges with linearly fused norbornane-bicyclo[2.2.0]hexane moieties through execution of the tandem Mitsudo-Smith series of reactions. The X-ray structure of the dimethoxybenzene-bridge-C-60 system 3a reveals favorable self-complementarity manifested by the unusual packing structure of 3a in the crystal. Molecular mechanics, semiempirical, and ab initio conformational analyses of compounds 2e, 3a, 3b, 3e, 3f, 3h, 68, and 70 (MM2, Sybyl, CVFF, AM1, HF/3-21G) were performed to quantify their ability to adopt two nondegenerate boat conformations, i.e,, extended and folded conformers, as well as their kinetic barrier of interconversion. A similar treatment of the C-60-bridge-C-60 system 4 revealed unusual preference for the folded-folded conformer (18.9 kcal/mol at CVFF level), which was not reproduced by the AM1 method (0.11 kcal/mol). The reduction potentials of the systems 2e, 3a, and 3e were about 0.1-0.5 V more negative than C-60, and the third reduction potential (E(3)) Of the 6-bond system 2e was 0.14 V more negative than the corresponding wave for the 10-bond system 3e. This shift was attributed to the closer proximity of the dimethylaniline donor group to the C-60 surface for 2e vs 3e.
    DOI:
    10.1021/jo960512p
  • 作为产物:
    描述:
    dimethyl (2aα,3β,8β,8aα)-2a,3,8,8a-tetrahydro-3,8-methano-4,7-dimethoxycyclobutanaphthalene-1,2-dicarboxylate四环庚烷 反应 72.0h, 以72%的产率得到dimethyl (1α,4α,4aβ,4bα,4cβ,5α,10α,10aβ,10bα,10cβ)-1,4,4a,4b,4c,5,10,10a,10b,10c-decahydro-1,4:5,10-dimethano-6,9-dimethoxybenzo<3',4'>cyclobuta<1',2':3,4>cyclobuta<1,2-b>naphthalene-4b,10b-dicarboxylate
    参考文献:
    名称:
    Antolovich, Michael; Oliver, Anna M.; Paddon-Row, Michael N., Journal of the Chemical Society. Perkin transactions II, 1989, p. 783 - 790
    摘要:
    DOI:
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文献信息

  • Synthesis and structural characterization of a novel pair of rigid diastereomeric triads
    作者:James M. Lawson、Donald C. Craig、Anna M. Oliver、Michael N. Paddon-Row
    DOI:10.1016/0040-4020(95)00107-j
    日期:1995.3
    A method is described for constructing totally rigid triad (nichromophoric) systems, D2-B1-D1-B2-A, in which the chromophores D2 (= dimethylaniline), D1 (= 1,4-dimethoxynaphthalene), and A (= dicyanovinyl) are fused to rigid hydrocarbon bridges, B1 and B2, comprising linearly fused norbornane and bicyclo[2.2.0]hexane units.
    描述了一种用于构建完全刚性的三联体(发色团)系统D 2 -B 1 -D 1 -B 2 -A的方法,其中发色团D 2(=二甲基苯胺),D 1(= 1,4-二甲氧基萘),和A(=二基ovyl)稠合到刚性烃桥B 1和B 2,其包括线性稠合的降冰片烷和双环[2.2.0]己烷单元。
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