250295
1,8-二碘辛烷
98%, contains copper as stabilizer
别名:
亚辛基二碘化物
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关于此项目
线性分子式:
I(CH2)8I
化学文摘社编号:
分子量:
366.02
Beilstein:
1735437
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
98%
表单
liquid
包含
copper as stabilizer
折射率
n20/D 1.5653 (lit.)
沸点
167-169 °C/6 mmHg (lit.)
密度
1.84 g/mL at 25 °C (lit.)
官能团
iodo
SMILES字符串
ICCCCCCCCI
InChI
1S/C8H16I2/c9-7-5-3-1-2-4-6-8-10/h1-8H2
InChI key
KZDTZHQLABJVLE-UHFFFAOYSA-N
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应用
1,8-二碘辛烷已用作加工添加剂以：
- 基于区域规整聚 3-己基噻吩和可溶性富勒烯衍生物改善体异质结太阳能电池的形貌和效率
- 提高聚合物太阳能电池的能量转换效率
危险声明
预防措施声明
危险分类
Aquatic Chronic 4
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Wang Li et al.
ACS applied materials & interfaces, 9(32), 27083-27089 (2017-07-27)
The development of simple and water-/alcohol-soluble interfacial materials is crucial for the cost-effective fabrication process of polymer solar cells (PSCs). Herein, highly efficient PSCs are reported employing water-/alcohol-soluble and low-cost rhodamines as cathode interfacial layers (CILs). The results reveal that
Zelin Li et al.
Small (Weinheim an der Bergstrasse, Germany), 14(16), e1704491-e1704491 (2018-03-24)
In recent years, rapid advances are achieved in polymer solar cells (PSCs) using nonfullerene small molecular acceptors. However, no research disclosing the influence of molecular weight (Mn ) of conjugated polymer on the nonfullerene device performance is reported. In this
Chengkai Xia et al.
Polymers, 12(8) (2020-08-14)
In this study, a solution-processable compact vanadium oxide (V2O5) film with a globular nanoparticulate structure is introduced to the hole transport layer (HTL) of polymer bulk-heterojunction based solar cells comprised of PTB7:PC70BM by using a facile metal-organic decomposition method to
Jihee Kim et al.
Polymers, 12(11) (2020-11-11)
Photostability of small-molecule (SM)-based organic photovoltaics (SM-OPVs) is greatly improved by utilizing a ternary photo-active layer incorporating a small amount of a conjugated polymer (CP). Semi-crystalline poly[(2,5-bis(2-hexyldecyloxy)phenylene)-alt-(5,6-difluoro-4,7-di(thiophen-2-yl)benzo[c][1,2,5]thiadiazole)] (PPDT2FBT) and amorphous poly[(2,5-bis(2-decyltetradecyloxy)phenylene)-alt-(5,6-dicyano-4,7-di(thiophen-2-yl)benzo[c][1,2,5]thiadiazole)] (PPDT2CNBT) with similar chemical structures were used for preparing
Ignasi Burgués-Ceballos et al.
ChemSusChem, 8(24), 4209-4215 (2015-12-15)
The application of conjugated materials in organic photovoltaics (OPVs) is usually demonstrated in lab-scale spin-coated devices that are processed under controlled inert conditions. Although this is a necessary step to prove high efficiency, testing of promising materials in air should
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