Bis(1,5-cyclooctadiene)rhodium(I) tetrakis[bis(3,5-trifluoromethyl)phenyl]borate

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Reagent Code: #152392
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CAS Number 404573-66-6

science Other reagents with same CAS 404573-66-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1182.5 g/mol
Formula C₄₈H₃₆BF₂₄Rh-
badge Registry Numbers
MDL Number MFCD10567026
thermostat Physical Properties
Melting Point 175 °C(decomp)
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Widely used as a catalyst precursor in homogeneous catalysis, particularly in olefin polymerization and asymmetric hydrogenation reactions. Its rhodium center, stabilized by cyclooctadiene ligands and a non-coordinating borate anion, creates a highly active and selective cationic complex. This makes it effective in promoting C–C bond formation and enabling high enantioselectivity in the synthesis of chiral molecules, which is valuable in pharmaceutical and fine chemical industries. The electron-deficient borate counterion enhances catalyst solubility and stability in nonpolar media, improving performance in industrial processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿7,380.00
inventory 100mg
10-20 days ฿17,520.00
inventory 250mg
10-20 days ฿26,260.00
inventory 1g
10-20 days ฿65,600.00

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Bis(1,5-cyclooctadiene)rhodium(I) tetrakis[bis(3,5-trifluoromethyl)phenyl]borate
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Widely used as a catalyst precursor in homogeneous catalysis, particularly in olefin polymerization and asymmetric hydrogenation reactions. Its rhodium center, stabilized by cyclooctadiene ligands and a non-coordinating borate anion, creates a highly active and selective cationic complex. This makes it effective in promoting C–C bond formation and enabling high enantioselectivity in the synthesis of chiral molecules, which is valuable in pharmaceutical and fine chemical industries. The electron-deficient

Widely used as a catalyst precursor in homogeneous catalysis, particularly in olefin polymerization and asymmetric hydrogenation reactions. Its rhodium center, stabilized by cyclooctadiene ligands and a non-coordinating borate anion, creates a highly active and selective cationic complex. This makes it effective in promoting C–C bond formation and enabling high enantioselectivity in the synthesis of chiral molecules, which is valuable in pharmaceutical and fine chemical industries. The electron-deficient borate counterion enhances catalyst solubility and stability in nonpolar media, improving performance in industrial processes.

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