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Merck
CN

337498

1,5-环辛二烯(吡啶)(三环己基磷化氢)铱六氟磷酸盐

85%

别名:

Crabtree 催化剂, [Ir(cod)(PCy3)(py)]PF6, 六氟磷酸(三环己基膦)(1,5-环辛二烯)(吡啶)合铱, 铱(I)六氟磷酸(1,5-环辛二烯)-(吡啶)-(三环己基膦)复合物

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关于此项目

经验公式(希尔记法):
C31H50F6IrNP2
化学文摘社编号:
分子量:
804.89
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
MDL number:
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产品名称

1,5-环辛二烯(吡啶)(三环己基磷化氢)铱六氟磷酸盐, 85%

InChI

1S/C18H33P.C8H12.C5H5N.F6P.Ir/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-2-4-6-8-7-5-3-1;1-2-4-6-5-3-1;1-7(2,3,4,5)6;/h16-18H,1-15H2;1-2,7-8H,3-6H2;1-5H;;/q;;;-1;+1/b;2-1-,8-7-;;;

SMILES string

[Ir+].c1ccncc1.F[P-](F)(F)(F)(F)F.C2CC=CCCC=C2.C3CCC(CC3)P(C4CCCCC4)C5CCCCC5

InChI key

UJXHUUQZACSUOG-KJWGIZLLSA-N

assay

85%

reaction suitability

core: iridium
reagent type: catalyst

mp

175 °C (dec.) (lit.)

Quality Level

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Application

均相氢化反应催化剂,硼氢化反应催化剂。
用于烯烃加氢、异构化和硼氢化的催化剂;也用于氢同位素交换反应。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Evans, D. A.; Fu, G. C.
Journal of the American Chemical Society, 113, 4042-4042 (1991)
Journal of the American Chemical Society, 114, 6671-6671 (1992)
Chemical Reviews, 93, 1331-1331 (1993)
Song, Z.; Hsung, R. P. et al.
Journal of Labelled Compounds & Radiopharmaceuticals, 50, 519-519 (2007)
Stereoselective synthesis of Boc-protected cis and trans-4-trifluoromethylprolines by asymmetric hydrogenation reactions.
Juan R Del Valle et al.
Angewandte Chemie (International ed. in English), 41(9), 1600-1602 (2002-05-03)

相关内容

The Crabtree Group developed the [(cod)IrLL']PF6 series of catalysts, where L is a P-donor such as PCy3 and L' and N-donor such as pyridine. These are very active in the hydrogenation of sterically hindered alkenes. The catalyst also shows directing effects as a result of binding of the catalyst to suitable functional groups on the substrate, followed by addition of H2 from the same side of the substrate that the functional group is located. Two versions of the catalyst are available from us one with PF6 and the other with BArF4 counteranion.

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