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[P(C6H5)3]2IrH2(CO)I is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27476-68-2

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27476-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27476-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,4,7 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27476-68:
(7*2)+(6*7)+(5*4)+(4*7)+(3*6)+(2*6)+(1*8)=142
142 % 10 = 2
So 27476-68-2 is a valid CAS Registry Number.

27476-68-2Downstream Products

27476-68-2Relevant academic research and scientific papers

Kinetic and mechanistic examination of NBu4[IrH2(CO)2I2] and NBu4[RhH2(CO)2I2] via para-hydrogen enhanced NMR spectroscopy

Hasnip, Sarah K.,Duckett, Simon B.,Taylor, Diana R.,Barlow, Graham K.,Taylor, Mike J.

, p. 889 - 890 (1999)

para-Hydrogen enhanced NMR signals are used to show that NBu4[M(CO)2I2](M = Rh, Ir) add hydrogen to form NBu4-{all-cis-[M(H)2(CO)2I2]} which for M = Ir undergoes H2 elimination in a step where ΔH≠ 106 ± 10 kJ mol-1 and ΔS≠ 60 ± 6 J K-1 mol-1 while showing a rich substitution chemistry with PPh3 that leads to both charged and neutral products via square pyramidal Ir(H)2(CO)2I.

Photochemical pump and NMR probe to monitor the formation and kinetics of hyperpolarized metal dihydrides

Procacci, Barbara,Aguiar, Pedro M.,Halse, Meghan E.,Perutz, Robin N.,Duckett, Simon B.

, p. 7087 - 7093 (2016/11/23)

On reaction of IrI(CO)(PPh3)21with para-hydrogen(p-H2),Ir(H)2I(CO)(PPh3)22 is formed which exhibits strongly enhanced 1H NMR signals for its hydride resonances. Complex 2 also shows similar enhancement of its NMR spectra when it is irradiated under p-H2. We report the use of this photochemical reactivity to measure the kinetics of H2 addition by laser-synchronized reactions in conjunction with NMR. The single laser pulse promotes the reductive elimination of H2 from Ir(H)2I(CO)(PPh3)22 in C6D6 solution to form the 16-electron precursor 1, back reaction with p-H2 then reforms 2 in a well-defined nuclear spin-state. The build up of this product can be followed by incrementing a precisely controlled delay (τ), in millisecond steps, between the laser and the NMR pulse. The resulting signal vs. time profile shows a dependence on p-H2 pressure. The plot of kobs against p-H2 pressure is linear and yields the second order rate constant, k2, for H2 addition to 1 of (3.26 ± 0.42) × 102 M?1 s?1. Validation was achieved by transient-UV-vis absorption spectroscopy which gives k2 of (3.06 ± 0.40) × 102 M?1 s?1. Furthermore, irradiation of a C6D6 solution of 2 with multiple laser shots, in conjunction with p-H2 derived hyperpolarization, allows the detection and characterisation of two minor reaction products, 2a and 3, which are produced in such low yields that they are not detected without hyperpolarization. Complex 2a is a configurational isomer of 2, while 3 is formed by substitution of CO by PPh3

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