GB892142A - Preparing metal carbonyls - Google Patents

Preparing metal carbonyls

Info

Publication number
GB892142A
GB892142A GB40501/58A GB4050158A GB892142A GB 892142 A GB892142 A GB 892142A GB 40501/58 A GB40501/58 A GB 40501/58A GB 4050158 A GB4050158 A GB 4050158A GB 892142 A GB892142 A GB 892142A
Authority
GB
United Kingdom
Prior art keywords
molybdenum
hexacarbonyl
chromium
vanadium
tungsten
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB40501/58A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ethyl Corp
Original Assignee
Ethyl Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ethyl Corp filed Critical Ethyl Corp
Publication of GB892142A publication Critical patent/GB892142A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G1/00Methods of preparing compounds of metals not covered by subclasses C01B, C01C, C01D, or C01F, in general
    • C01G1/04Carbonyls

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

Abstract

Carbonyls of metals of Group Vb and VIb, e.g. vanadium, chromium, molybdenum and tungsten, are prepared by reacting a salt, oxide, sulphide, alcoholate or phenate of the metal in question with carbon monoxide and a stable organo compound of a group IIb or IIIa element, e.g. Zn, Cd, Hg, B, Al, Ga, In or Tl. Organo compounds specified include dimethylzinc, di-isopropyl-zinc, dioctylzinc, methylethylzinc, n-heptyl-n-octylzinc, n-butylzinc bromide, ethylzinc hydride, dicyclohexylzinc, sodium zinc triethyl, diphenylzinc, diethylcadmium, diethylmercury, dibenzylmercury, triethylboron, ethylborondifluoride, sodium tetraethylborate, methyldiethylaluminium, tri-isooctyl-aluminium, methylethyloctylaluminium, diethylaluminium hydride, octylaluminium dihydride, lithium aluminium tetraethyl, potassium aluminium dioctyl dihydride, dimethylaluminium chloride, ethylaluminium sesquichloride, tripropylgallium, trimethylindium, triphenylaluminium, sodium aluminium diethyl acetylide, and triethylthallium. In Example I, a mixture of chromium trioxide, diethylzinc, and diethyl ether in an inert atmosphere of nitrogen is pressurized with 2,500 p.s.i.g. of CO and heated to 100 DEG C. with continuous agitation for four hours. After cooling to 30 DEG C., the mixture is quenched with dilute HCl, and chromium hexacarbonyl is recovered. In Examples II and III, molybdenum hexacarbonyl is obtained using diethylzinc, tetrahydrofuran, and molybdenum trichloride or trioxide, in Example IV tungsten hexacarbonyl is similarly obtained, in Example V vanadium petacarbonyl dimer is similarly obtained using diphenylzinc, and in Example VI chromium hexacarbonyl is obtained from chromons acetylacetate. In Example VII, vanadium pentacarbonyl is obtained using vanadium dichloride, diethylaluminium hydride and diethyl ether. In Examples IX and X, chromium hexacarbonyl is prepared using triethylaluminium and either chromons acetylacetate and tetrahydrofuran or chromic chloride and diethyl ether. In Example XI, molybdenum hexacarbonyl is obtained from molybdenum dichloride, triethylaluminium and diethyl ether. Examples XII and XIII are similar, producing tungsten and molybdenum hexacarbonyls from tungsten and molybdenum trioxides. Numerous other organic diluents, which are hydrocarbons, ethers, amines, pyridines, and isoquinoline.
GB40501/58A 1957-12-23 1958-12-16 Preparing metal carbonyls Expired GB892142A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US892142XA 1957-12-23 1957-12-23

Publications (1)

Publication Number Publication Date
GB892142A true GB892142A (en) 1962-03-21

Family

ID=22216358

Family Applications (1)

Application Number Title Priority Date Filing Date
GB40501/58A Expired GB892142A (en) 1957-12-23 1958-12-16 Preparing metal carbonyls

Country Status (2)

Country Link
DE (1) DE1113688B (en)
GB (1) GB892142A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102070180A (en) * 2010-12-07 2011-05-25 吉林吉恩镍业股份有限公司 Method for synthesizing hexacarbonyl tungsten or molybdenum complex

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE518781C (en) * 1928-07-05 1931-02-19 I G Farbenindustrie Akt Ges Process for the production of metal carbonyls
GB323021A (en) * 1928-08-18 1929-12-18 Ig Farbenindustrie Ag Improvements in the manufacture and production of metal carbonyls
DE531479C (en) * 1930-02-13 1931-08-10 Ig Farbenindustrie Ag Process for the production of metal carbonyls
US2803525A (en) * 1955-04-04 1957-08-20 Union Carbide Corp Process for preparing chromium carbonyl

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102070180A (en) * 2010-12-07 2011-05-25 吉林吉恩镍业股份有限公司 Method for synthesizing hexacarbonyl tungsten or molybdenum complex

Also Published As

Publication number Publication date
DE1113688B (en) 1961-09-14

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