726192
Bis(4-methylphenyl)iodonium hexafluorophosphate
98%
๋์์ด(๋ค):
Bis(p-tolyl)iodonium hexafluorophosphate
๋ก๊ทธ์ธ์กฐ์ง ๋ฐ ๊ณ์ฝ ๊ฐ๊ฒฉ ๋ณด๊ธฐ
๋ชจ๋ ์ฌ์ง(1)
About This Item
์คํ์(Hill ํ๊ธฐ๋ฒ):
C14H14F6IP
CAS Number:
Molecular Weight:
454.13
Beilstein:
3581445
EC Number:
MDL number:
UNSPSC ์ฝ๋:
12352300
PubChem Substance ID:
NACRES:
NA.23
์ถ์ฒ ์ ํ
Quality Level
๋ถ์
≥97.5% (TLC)
98%
์์
solid
SMILES string
F[P-](F)(F)(F)(F)F.Cc1ccc([I+]c2ccc(C)cc2)cc1
InChI
1S/C14H14I.F6P/c1-11-3-7-13(8-4-11)15-14-9-5-12(2)6-10-14;1-7(2,3,4,5)6/h3-10H,1-2H3;/q+1;-1
InChI key
LHLVGWWCRPPKBC-UHFFFAOYSA-N
๊ด๋ จ ์นดํ ๊ณ ๋ฆฌ
์ผ๋ฐ ์ค๋ช
Bis(4-methylphenyl)iodonium hexafluorophosphate is a white powder. It melts at 175-180 ยฐC and shows an UV absorption peak at 267nm. 1
์ ํ๋ฆฌ์ผ์ด์
- Covalent Functionalisation of Few-Layer Black Phosphorus using Aryl Iodonium Salts and Comparison to Diazonium Modified Black Phosphorus: Explores the functionalization of black phosphorus using bis(4-methylphenyl)iodonium hexafluorophosphate and compares it to diazonium modification (M Van Druenen, 2019).
- Iodonium sulfonates as highโperformance coinitiators and additives for CQโbased systems: Toward aromatic amineโfree photoinitiating systems: Examines the effectiveness of iodonium sulfonates and bis(4-methylphenyl)iodonium hexafluorophosphate in CQ-based photoinitiating systems (J Kirschner et al., 2019).
- Thiophene-substituted phenothiazine-based photosensitisers for radical and cationic photopolymerization reactions under visible laser beams (405 and 455 nm): Studies the use of thiophene-substituted phenothiazine in combination with bis(4-methylphenyl)iodonium hexafluorophosphate for effective photopolymerization (P Chao et al., 2016).
์ ํธ์ด
Danger
์ ํด ๋ฐ ์ํ ์ฑ๋ช ์
์๋ฐฉ์กฐ์น ์ฑ๋ช ์
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (ยฐF)
Not applicable
Flash Point (ยฐC)
Not applicable
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