Chromium carbonyl synthesis

FT-ICR, see Fourier-transform ion cyclotron resonance Fullerene[60], germanium-germanium addition, 10, 748 Fullerenes with cobalt, 7, 51 on cobalt Cp rings, 7, 73 inside metallodendrimers, 12, 401 microwave applications, 1, 334 Pd rc-complexes, 8, 348 Ru—Os complexes, 6, 830 with tungsten carbonyls, 5, 687 )2-Fullerenes, with platinum, 8, 634 Fulvalene actinide complex, synthesis, 4, 232 Fulvalene chromium carbonyls, synthesis and characteristics, 5, 264... 

Fulvalene zirconium(III) compounds, reactions, 4, 751 Fulvene chromium carbonyls, synthesis and characteristics,... 

The nitrogen complex had already been synthesized in a solid matrix, but its decomposition kinetics and its further photolysis could be studied only in solution. The liquid noble gas technique is superior to the solid matrix technique, especially for the synthesis of multiple substituted chromium carbonyl nitrogen complexes. Their IR spectra were extremely complex in matrices, due to "site splittings" which arise when different molecules are trapped in different matrix environments /18/. 

Diphosphaferrocene, with chromium carbonyls, 5, 220 l,l -Diphospha[2]ferrocenophane, synthesis, 6, 210 Diphosphazanes, in dinuclear Ru complexes, 6, 674 l,l -Diphosphetanylferrocenes, preparation, 6, 200-201 Diphosphine borane complex, polypyrrole support for,... 

Electric arcs, in metal vapor synthesis, 1, 224 Electric-field-induced second harmonic generation Group 8 metallocenes, 12, 109 for hyperpolarizability measurement, 12, 107 Electrochemical cell assembly, in cyclic voltammetry, 1, 283 Electrochemical irreversibility, in cyclic voltammetry, 1, 282 Electrochemical oxidation, arene chromium carbonyls, 5, 258 Electrochemical properties, polyferrocenylsilanes, 12, 332 Electrochemical reduction, bis-Cp Zr(III) and (IV) compounds, 4, 745 Electrochemical sensors biomolecule—ferrocene conjugates... 

Ferrocenyl ligands, via zinc reagents, 9, 120 Ferrocenylmethyl phosphonium salts, with gold(I), 2, 274 Ferrocenylmonophosphine, in styrene asymmetric hydrosilylation, 10, 817 Ferrocenyl oxazolines, synthesis, 6, 202 Ferrocenylphosphines with chromium carbonyls, 5, 219 in 1,3-diene asymmetric hydrosilylation, 10, 824-826 preparation, 6, 197 various complexes, 6, 201 Ferrocenylselenolates, preparation, 6, 188 Ferrocenyl-substituted anthracenes, preparation, 6, 189 Ferrocenyl terpyridyl compounds, phenyl-spaced, preparation 6, 188 Ferrocifens... 

Heteroalkenes, with iron, 6, 132 Heteroannulation, allylic benzylamines, 10, 156 Heteroarene chromium carbonyls, preparation and characteristics, 5, 260 Heteroarenes borylation, 10, 242 C—H functionalizations, 10, 127 as metal vapor synthesis milestone, 1, 237 with titanium, 4, 246 vanadium complexes, 5, 48 7]6-Heteroarenes, with platinum, 8, 664 Heteroaromatic compounds... 

Heterometal alkoxide precursors, for ceramics, 12, 60-61 Heterometal chalcogenides, synthesis, 12, 62 Heterometal cubanes, as metal-organic precursor, 12, 39 Heterometallic alkenes, with platinum, 8, 639 Heterometallic alkynes, with platinum, models, 8, 650 Heterometallic clusters as heterogeneous catalyst precursors, 12, 767 in homogeneous catalysis, 12, 761 with Ni—M and Ni-C cr-bonded complexes, 8, 115 Heterometallic complexes with arene chromium carbonyls, 5, 259 bridged chromium isonitriles, 5, 274 with cyclopentadienyl hydride niobium moieties, 5, 72 with ruthenium—osmium, overview, 6, 1045—1116 with tungsten carbonyls, 5, 702 Heterometallic dimers, palladium complexes, 8, 210 Heterometallic iron-containing compounds cluster compounds, 6, 331 dinuclear compounds, 6, 319 overview, 6, 319-352... 

Linear polarization, and NLO properties, 12, 102 Linear polymers, siloxanes, synthesis, 3, 660 Linkage isomerism, for photochromic behavior, 1, 245 Linked cages, metallacarboranes, 3, 245 Linkers, traceless, chromium carbonyls as, 5, 251 Lipids, in bioorganometallic chemistry, 1, 904 Liquefied noble gases, in low-temperature infrared studies, 1, 264... 

The diverse chemistry of chromium carbonyl complexes has its origin in the discovery of Cr(CO)6 in 1926 by Job and Cassal. Early developments in this area included the preparation of the (jj -arene)Cr(CO)3 family of organometallics by Nicholls and Whiting in 1959, the synthesis of the first structurally characterized carbene complex by Fischer and Maasbdl (1965), and a... 

Crystal-structure determinations performed on chromium carbonyl carbynes indicate an average Cr C bond length of 1.70 A, ca. 0.2 A shorter than the average Cr C(carbonyl) distance. An exception is seen in X(CO)4Cr=C-NR2, in which the Cr-C bond is somewhat longer and the C N bond somewhat shorter than expected. These findings are consistent with the presence of some double bond character. The Cr C-R bond angle is customarily very close to linear, but structures bent up to 12° are known. Chromium carbonyl carbynes are frequently employed as starting materials for the synthesis of carbenes inaccessible... 

In 1954 a new synthesis for chromium carbonyl was developed in collaboration wdth W. Hafner. The system CrCls/AlCla/Al/CeHe/CO used in this case was found, when the reaction was more closely studied, to open the way to the compound CrfCgHels 53). It was shown that in an autoclave at 180°, without the carbon monoxide, a mixture resulted which contained the [Cr (CeH8)2] cation, produced as followrs ... 

Schlogl K (1989) Stereochemistry of arenetricarbonylchromium complexes—useful intermediates for stereoselective synthesis. In Werner H, Erker G (eds) Organometal-lics in organic synthesis 2. Springer, Berlin Heidelberg New York, p 63 Solladi -Cavallo A (1989) Chiral arene-chromium-carbonyl complexes in asymmetric synthesis. In Liebeskind LS (ed) Advances in metal organic chemistry, vol 1. Jai Press, London, p 99... 

A recent synthesis of this building block has been published by Eastham et al. in 2006 (48). Their key step is a Dotz benzannulation reaction and is shown in Scheme 2.10. The bromohydrin 66 was formed from dihydrofuran (50). Cobalt-mediated cyclization, followed by ozonolysis with reductive work-up yielded 68 after hydrazine formation. Reductive removal of the hydrazine function, followed by chromium-carbonyl formation gave the Dotz reaction precursor 69. This reacted with an alkyne in the Dotz reaction, and was then oxidized and hydrogenated 70). Pyrolysis gave the protected alcohol and the remaining free alcohol was protected as a triflate (—> 71). Reductive removal of the triflate and deprotection of the silyl ether yielded the desired 33 in 1.2% overall yield. 

It has been observed that in basic media aromatic hydrocarbons and benzylmethyl ethers bound to -Cr(CO)3 are easily nitrosated at the benzylic position. A review type article discusses the stereoselective manipulation of acetals derived from o-substituted benzaldehyde chromium tricarbonyls. The diastereoselective synthesis of a range of substituted cyclohexadienes has been reported from enandomerically pure (2-phenyl-4,S-dibydroxazole)chromium tiicaibonyl complexes. Aromatic nucleophilic substitution on halaogenoarene tricarbonylchromium complexes gives rise to a series of complexed aniline derivatives. The diastereoselective 1,4-addition of organocuprates to o-substituted-phenyI-(E)-enone chromium carbonyl conq)lexes provides a new method for remote stereocontrol at the 1,3, and S-positimis of the side chains. ... 

An overview of the effect of catalyst in the reaction of arenes with chromium hexacarbrmyl has been published. The reactivity of 17-, 18-, and 19-etectron catkMis generated electrochemically from mesitylene-tungsten tricarbonyl has been examined. The gas phase ion chemistry of a range of arene tricarbonylchromium complexes has been investigated by F.T. mass spectrometry. An improved synthesis of substituted naphthalene chromium carbonyls has appeared. ... 

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