摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1,5-Diphenyl-quadricyclan | 31197-95-2

中文名称
——
中文别名
——
英文名称
1,5-Diphenyl-quadricyclan
英文别名
1,5-Diphenyltetracyclo[3.2.0.02,7.04,6]heptane
1,5-Diphenyl-quadricyclan化学式
CAS
31197-95-2
化学式
C19H16
mdl
——
分子量
244.336
InChiKey
KQPJPVOMVWKELG-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):
    4.4
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Diaryl-substituted norbornadienes with red-shifted absorption for molecular solar thermal energy storage
    摘要:
    将降冰片二烯(NBDs)的吸收红移到可见光区域,可使 NBDs 在阳光的驱动下光异构化为四环(QCs)。这对于利用 NBD-QC 系统进行分子太阳能热(MOST)储能是非常必要的。本文报告了对五种二芳基取代的降冰片二烯的研究。引入的芳基使降冰片二烯的紫外/可见吸收光谱发生了显著的红移,使用太阳能模拟装置进行的设备实验证明了这些化合物用于 MOST 储能的潜力。
    DOI:
    10.1039/c3cc47517d
  • 作为产物:
    描述:
    2,3-diphenylbicyclo[2.2.1]hepta-2,5-diene氘代二甲亚砜 为溶剂, 反应 0.03h, 以100%的产率得到1,5-Diphenyl-quadricyclan
    参考文献:
    名称:
    Diaryl-substituted norbornadienes with red-shifted absorption for molecular solar thermal energy storage
    摘要:
    将降冰片二烯(NBDs)的吸收红移到可见光区域,可使 NBDs 在阳光的驱动下光异构化为四环(QCs)。这对于利用 NBD-QC 系统进行分子太阳能热(MOST)储能是非常必要的。本文报告了对五种二芳基取代的降冰片二烯的研究。引入的芳基使降冰片二烯的紫外/可见吸收光谱发生了显著的红移,使用太阳能模拟装置进行的设备实验证明了这些化合物用于 MOST 储能的潜力。
    DOI:
    10.1039/c3cc47517d
点击查看最新优质反应信息

文献信息

  • Diaryl-substituted norbornadienes with red-shifted absorption for molecular solar thermal energy storage
    作者:Victor Gray、Anders Lennartson、Phasin Ratanalert、Karl Börjesson、Kasper Moth-Poulsen
    DOI:10.1039/c3cc47517d
    日期:——
    Red-shifting the absorption of norbornadienes (NBDs), into the visible region, enables the photo-isomerization of NBDs to quadricyclanes (QCs) to be driven by sunlight. This is necessary in order to utilize the NBD–QC system for molecular solar thermal (MOST) energy storage. Reported here is a study on five diaryl-substituted norbornadienes. The introduced aryl-groups induce a significant red-shift of the UV/vis absorption spectrum of the norbornadienes, and device experiments using a solar-simulator set-up demonstrate the potential use of these compounds for MOST energy storage.
    将降冰片二烯(NBDs)的吸收红移到可见光区域,可使 NBDs 在阳光的驱动下光异构化为四环(QCs)。这对于利用 NBD-QC 系统进行分子太阳能热(MOST)储能是非常必要的。本文报告了对五种二芳基取代的降冰片二烯的研究。引入的芳基使降冰片二烯的紫外/可见吸收光谱发生了显著的红移,使用太阳能模拟装置进行的设备实验证明了这些化合物用于 MOST 储能的潜力。
查看更多

同类化合物

3,4-双(4-羟基苯基)环丁烷-1,2-二羧酸 3,4-二苯基环丁烷-1,2-二羧酸 1-[2,3-二甲基-4-(2,4,5-三甲氧基苯基)环丁基]-2,4,5-三甲氧基苯 (2,3,4-三苯基环丁基)苯 DL-(1R,2R,3S,4S)-3,4-bis(4-methoxyphenyl)cyclobutane-1,2-dicarboxylic acid tetrakis-1,2,3,4-(4’- carboxyphenyl)cyclobutane 3,3'-dinitro-β-truxinic acid diphenyl 3,4-diphenylcyclobutane-1,2-dicarboxylate DL-(1R,2R,3S,4S)-diphenyl 3,4-diphenylcyclobutane-1,2-dicarboxylate 3,4-bis(2-hydroxy-5-methylphenyl)cyclobutane-1,2-dicarboxylic acid N-(n-pentyl)-3β,4β-bis(3',4'-dimethoxyphenyl)-1α,2α-cyclobutanedicarboximide trans-1,2-diphenylbicyclo[3.1.0.02,4]hexane 8β,8'α-dimethyl-7α,7'β-bis(3-methoxy-4-hydroxyphenyl)cyclobutane 4,4'-((1R,2R,3S,4S)-3,4-dimethylcyclobutane-1,2-diyl)bis(methoxybenzene) caracasandiamide 3β,4β-bis(3',4'-dimethoxyphenyl)-1α-carboxy-2α-<butyl>cylobutanecarboxamide quinic acid diester of 3,4,3',4'-tetrahydroxy-β-truxinic acid 3,3′-difluoro-β-truxinic acid endiandrin B 3,3-Dimethyl-2,4-diphenyl-tricyclo[3.2.0.02,4]heptane (1R,6S,7S,8R)-7,8-Diphenyl-bicyclo[4.2.0]octane 1,5-Diphenyl-quadricyclan dimethyl t-3,t-4-di-(3,4,5-trimethoxyphenyl)cyclobutane-r-1,c-2-dicarboxylate (±)-(1R,5S,6R,7S)-6,7-bis(4-methoxyphenyl)-3-oxabicyclo[3.2.0]heptane 2-((1R,2S,3R,4R)-2-methyl-2-nitro-3,4-diphenylcyclobutyl)acetaldehyde 1α,2α-Di-(2-methoxy-phenyl)-cyclobutan-dicarbonsaeure-(3β,4β)-dimethylester o,o'-Dimethyl-β-truxillsaeuredimethylester 1,2-diisobutyryl-3,4-diphenyl-cyclobutane 3,4-bis(3,4-dimethylphenyl)cyclobutane-1,2-dicarboxylic acid (17S,18R,19S,20R)-18,19-bis(3,4-dimethylphenyl)-15,22-diazahexacyclo[21.2.2.211,14.12,6.017,20.010,30]triaconta-1(25),2,4,6(30),7,9,11(29),12,14(28),23,26-undecaene-16,21-dione 3,3-Dimethyl-2,4-diphenyl-endo-tricyclo<3.3.0.02,4>oct-6-en ((1S,2R,3S,4R)-3-Hydroxymethyl-1,4-diphenyl-bicyclo[2.2.0]hex-2-yl)-methanol (1R,7S,8R,11S)-8,11-Diphenyl-3,5-dioxa-4-thia-tricyclo[5.4.0.08,11]undecane 4,4-dioxide 4a,4b-Bis(4-methoxyphenyl)decahydrobiphenylene-1,8-dione 4a,4b-Bis(4-nitrophenyl)decahydrobiphenylene-1,8-dione 8-Methyl-4,4a-diphenyltetrahydro-1h,5h-3,4,4b-(methanetriyl)cyclopenta[1,3]cyclopropa[1,2-b]pyridin-2(3h)-one (1R,2R,3R,4R)-3,4-Bis-{2-[bis-(4-tert-butyl-phenyl)-phosphinoyl]-phenyl}-cyclobutane-1,2-dicarboxylic acid diethyl ester (S,S,S,S)-3,4-bis(2-diphenylphosphinylphenyl)-1,2-cyclobutanedimethyl di(diphenylphosphine) (1R,2R,3R,4R)-3,4-Bis-[2-(diphenyl-phosphinoyl)-phenyl]-cyclobutane-1,2-dicarboxylic acid diethyl ester (1R,2R,3R,4R)-3,4-Bis-{2-[bis-(3,5-dimethyl-phenyl)-phosphinoyl]-phenyl}-cyclobutane-1,2-dicarboxylic acid diethyl ester 4,4'-(3,4-diphenyl-cyclobutane-1,2-diyl)-bis-benzo[h]quinoline 4,4'-(3,4-diphenyl-cyclobutane-1,2-diyl)-bis-benzo[h]quinoline 3,4-diphenyl-3,4-dichlorocyclobutanodicarbox-1,2-dianilide (1S,5R,6R)-3-butyl-6,7-bis(2-hydroxyphenyl)-3-azabicyclo[3.2.0]heptane-2,4-dione (1R,2R,3R,4R)-3,4-Bis-{2-[bis-(4-methoxy-phenyl)-phosphinoyl]-phenyl}-cyclobutane-1,2-dicarboxylic acid diethyl ester 1,2-Diphenyl-1,2,2a,10b-tetrahydro-cyclobuta[l]phenanthrene all-cis-1,2-Dibenzyl-3,4-diphenylcyclobutan (3,4-diphenylcyclobutane-1,2-diyl)bis(phenylmethanone) 1,2-dibenzoyl-3,4-diphenyl-cyclobutane