产品名称
铑, foil, not light tested, 50x50mm, thickness 0.00025mm, permanent polyester support, 99.9%
InChI
1S/Rh
SMILES string
[Rh]
InChI key
MHOVAHRLVXNVSD-UHFFFAOYSA-N
assay
99.9%
form
foil
manufacturer/tradename
Goodfellow 823-663-42
resistivity
4.33 μΩ-cm, 20°C
size × thickness
50 x 50 mm × 0.00025 mm
bp
3727 °C (lit.)
mp
1966 °C (lit.)
density
12.41 g/cm3 (lit.)
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General description
For updated SDS information please visit www.goodfellow.com.
Legal Information
Product of Goodfellow
存储类别
13 - Non Combustible Solids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Vladimir V Grushin
Accounts of chemical research, 43(1), 160-171 (2009-10-01)
Although springing from two established fields, organometallic chemistry and fluorine chemistry, organometallic fluorine chemistry is still in its early stages. However, developments in this area are expected to provide new tools for the synthesis of selectively fluorinated organic compounds that
Jerzy Klosin et al.
Accounts of chemical research, 40(12), 1251-1259 (2007-11-14)
A series of bis-phosphite and bis-phosphine ligands for asymmetric hydroformylation reactions has been evaluated. Bis-phosphite ligands lead, in general, to high regioselectivities across a range of substrates while good enantioselectivities are limited to only a few examples. We found that
Jeremy M Praetorius et al.
Dalton transactions (Cambridge, England : 2003), (31)(31), 4079-4094 (2008-08-09)
The organometallic chemistry of N-heterocyclic carbene complexes of the transition metals has received significant attention over the past ten years, especially with respect to complexes of Pd and Ru. The present Perspective highlights the chemistry of NHC complexes of another
Pablo Etayo et al.
Chemical Society reviews, 42(2), 728-754 (2012-11-08)
During the last few decades, rhodium-catalysed asymmetric hydrogenation of diverse alkene classes has emerged as a powerful synthetic tool in the pharmaceutical industry, contributing to the manufacturing of chiral drugs, recent drug candidates for clinical trials, and major synthetic precursors
Jean Bouffard et al.
Topics in current chemistry, 292, 231-280 (2010-01-01)
A review is presented of synthetic methods for the preparation of biaryls by the rhodium-catalyzed C-H bond arylation of arenes with aryl halides (C-H/ C-X couplings), arylmetal reagents (C-H/C-M couplings) and arenes (C-H/C-H couplings), with an emphasis on postulated mechanisms
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