헥사페닐벤젠

헥사페닐벤젠
헥사페닐벤젠 구조식 이미지
카스 번호:
992-04-1
한글명:
헥사페닐벤젠
동의어(한글):
헥사페닐벤젠
상품명:
Hexaphenylbenzene
동의어(영문):
HEXAPHENYLBENZENE;Six phenyl benzene;Benzene, hexaphenyl-;Hexaphenylbenzene 98%;Hexaphenylbenzene, 98+%;1,2,3,4,5,6-Hexaphenylbenzene;1,2,3,4,5,6-hexakis-phenylbenzene;3',4',5',6'-tetraphenyl-o-terphenyl;m-Terphenyl, 2',4',5',6'-tetraphenyl-;3',4',5',6'-tetraphenyl-1,1':2',1''-terphenyl
CBNumber:
CB8389989
분자식:
C42H30
포뮬러 무게:
534.69
MOL 파일:
992-04-1.mol
MSDS 파일:
SDS

헥사페닐벤젠 속성

녹는점
>300 °C (lit.)
끓는 점
547.47°C (rough estimate)
밀도
0.8530 (rough estimate)
굴절률
1.4690 (estimate)
물리적 상태
powder to crystal
색상
흰색에서 밝은 노란색
수용성
물에 불용성.
BRN
1895903
안전
  • 위험 및 안전 성명
안전지침서 24/25-25-24
WGK 독일 3
HS 번호 29029090
그림문자(GHS):
신호 어:
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
예방조치문구:
NFPA 704
1
0 0

헥사페닐벤젠 C화학적 특성, 용도, 생산

화학적 성질

white to off-tan powder

용도

Hexaphenylbenzene was used to prepare the fluorescent nanorods used for the detection of trinitrotoulene (TNT).

주요 응용

Hexaphenylbenzene can be used as a starting material to synthesize:
1,2,3,4,5,6-Hexacyclohexylcyclohexane by Pd/C catalyzed hydrogenation reaction.
Stable hexatrityl cations and porous organic polymers for applications in catalysis and gas storage.
Hexa-peri-hexabenzocoronene via one-pot substitution and oxidative cyclodehydrogenation reaction in the presence of t-BuCl/FeCl3.
as a structural unit for the synthesis of polymers of intrinsic microporosity.

Synthesis

Hexaphenylbenzene has been prepared by heating tetraphenylcyclopentadienone and diphenylacetylene without solvent and by trimerization of diphenylacetylene with bis-(benzonitrile)-palladium chloride and other catalysts. The reaction proceeds via a Diels-Alder reaction to give the hexaphenyldienone, which then eliminates carbon monoxide.
synthesis of Hexaphenylbenzene
Multi-Step Synthesis of hexaphenylbenzene from benzil
Procedure: Add 0.8 g of tetraphenylcyclopentadienone, 0.8 g of diphenylacetylene (synthesized by you in CH 2270 lab last semester), and 4 g of benzophenone to a 25 mL round-bottom flask. Place a magnetic stir bar in the flask. Make sure no material lodges on the neck or walls of the flask. Attach the condenser to the round-bottom flask. Do not attach the hoses. The condenser will be used as an “air condenser” for this experiment. Heat the reaction mixture VERY HIGH with the sand bath on the hot plate/stirrer. Benzophenone is your solvent and its boiling point is over 300 °C! Heat the reaction mixture to reflux. Carbon monoxide is evolved, the purple color begins to fade in 15-20 minutes, and the color changes to a reddish brown in 25-30 minutes. When no further lightening in color is observed (after about 45 minutes), the heat is removed and 1 mL of diphenyl ether is added to prevent subsequent solidification of the benzophenone. The crystals that separate are brought into solution by reheating and the solution is let stand for crystallization at room temperature. The product is collected and washed free of brown solvent with toluene to give colorless plates.

헥사페닐벤젠 준비 용품 및 원자재

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