250295
1,8-Diiodooctane
98%, contains copper as stabilizer
Synonym(s):
Octamethylene diiodide
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About This Item
Linear Formula:
I(CH2)8I
CAS Number:
Molecular Weight:
366.02
Beilstein:
1735437
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
98%
form
liquid
contains
copper as stabilizer
refractive index
n20/D 1.5653 (lit.)
bp
167-169 °C/6 mmHg (lit.)
density
1.84 g/mL at 25 °C (lit.)
functional group
iodo
SMILES string
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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Application
1,8-Diiodooctane has been employed as processing additive:
- to improve the morphology and the efficiency of bulk heterojunctions solar cells, based on the regioregular poly(3-hexylthiophene) and a soluble fullerene derivative
- to improve the power conversion efficiency of polymer solar cells
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 4
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
Xing Fan et al.
Journal of nanoscience and nanotechnology, 14(5), 3592-3596 (2014-04-17)
Controlling the blend morphology is critical for achieving high power conversion efficiency in polymer/fullerene bulk heterojunction (BHJ) photovoltaic devices. As a simple and effective method to control morphology, adding processing additives has been widely applied in the organic BHJ solar
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
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