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Vanadocene diiodide, with the chemical formula (C5H5)2VI2, is an organometallic compound consisting of a vanadium atom sandwiched between two cyclopentadienyl rings, with two iodine atoms attached to the vanadium. vanadocene diiodide is a significant organometallic complex, known for its stability and unique electronic structure. It is often used as a precursor in the synthesis of various vanadium-containing compounds and as a catalyst in organic reactions. Vanadocene diiodide is also of interest in materials science due to its potential applications in the development of new materials with unique properties.

75102-54-4

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75102-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75102-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,0 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75102-54:
(7*7)+(6*5)+(5*1)+(4*0)+(3*2)+(2*5)+(1*4)=104
104 % 10 = 4
So 75102-54-4 is a valid CAS Registry Number.

75102-54-4Downstream Products

75102-54-4Relevant academic research and scientific papers

Activation of CO2-like molecules: Synthetic and structural studies on a η2-C,N metal-bonded carbodiimide and its conversion into a η2-C,N metal-bonded amidinyl ligand

Pasquali, Marco,Gambarotta, Sandro,Floriani, Carlo,Chiesi-Villa, Angiola,Guastini, Carlo

, p. 165 - 171 (2008/10/08)

Vanadocene reacts with p-tolylcarbodiimide (p-TCD) producing a metallaazacyctopropane-like complex Cp2V(RN-C=NR) (I) (R = p-CH3C6H4; Cp = η5-C5H5; vCN(Nujol) 1645 cm-1; μeff = 1.76 μB at 293.5 K). The X-ray analysis performed on complex I shows that vanadium is η5 bonded to the two Cp rings, which are in a bent arrangement, making a cavity in the equatorial plane for the CN2 unit. The C-N bond distances agree with the presence of a single C-N bond interacting with the metal and a free C=N double bond. Complex I reacts with both O2 and I2, releasing p-TCD. Coordinated p-TCD is converted in a η2-C,N metal-bonded trialkylamidinyl ligand by the action of CH3I on complex I. The reaction with CH3I, followed by the addition of I2, allowed isolation of [Cp2V(R(CH3)NC=NR)]I3 (II) (R = p-CH3C6H4; vCN(Nujol) 1680 cm-1; μeff = 1.78 μB at 293 K). The X-ray analysis showed an overall structure of the cation similar to that of I, with the amidinyl ligand acting as a three-electron-donor ligand and displaying a bonding mode similar to that observed for η2-C,O acyls and η2-C,N iminoacyls. The two C-N bond distances within the CN2 unit have a high double-bond character (1.26 (2) and 1.33 (2) A?), indicating a significant electronic delocalization all over the VCN2 unit with a carbenoid character for the carbon bonded to the vanadium atom. In both complexes, V-C bond distances (about 2.0 A?) fall in the expected range for a V-C (sp2) bond. Crystallographic details for complex I: space group Pna21 (orthorhombic); a = 14.446 (3) A?, b = 14.186 (2) A?, c = 20.903 (4) A?, V= 4283.7 A?3; Z = 8; Dcalcd = 1.251 g cm-3. The final R factor was 8.4% for 1439 observed reflections. Crystallographic details for complex II: space group P21/c (monoclinic); a = 14.260 (6) A?, b = 19.176 (5) A?, c = 10.628 (4) A?; β = 106.92 (5)°; V = 2780.4 A?3; Z = 4; Dcalcd = 1.910 g cm-3. The final R factor was 6.3% for 2283 observed reflections.

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