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Manganese complexes cyclopentadienyl

The reactions between cyclopropenes and carbon monoxide in the presence of transition metals have been of some use in synthesis,93 and in 1978 Binger initiated a study of the reactions between metal carbonyls and cyclopropenes in order to elucidate the generality of these reactions.75 It was found that dicarbonyl 775-cyclopentadienyl(tetrahydrofuran)manganese(I) reacted with 3,3-dime thy Icy clopropene at 0°C to produce -(vinylketene) complex 81 in fair yield. The only other transition metal in Binger s study that was found to react with 3,3-dimethylcyclopropene in this manner was iron (see Section VI,B). [Pg.297]

Manganese carbonyl, Mn2(CO)io, when treated with tetracyclone at 140-150°, gives an air-sensitive product which on hydrolysis gives the T-cyclopentadienyl complex (LII) 215). Manganese carbonyl does not react with dimcthylacetylene in sunlight, but duroquinone was formed in a similar reaction of the alkyne with [Mn(CO)6] 1 155). Mn(—1) is iso-electronic with Fe(0), and it is suggested that the unstable quinone com-... [Pg.119]

Alkyl-bridged cyclopentadienyl complexes, with manganese, 5,819... [Pg.45]

Manganese carbenes, preparation, 5, 825 Manganese carbonyl complexes with 776-arene complexes, 5, 787 cyclopentadienyl complexes, 5, 783 with hydrocarbon ligands, complexes, 5, 776 synthesis and characteristics, 5, 761 Manganese carbonyl halides, applications and reactivity,... [Pg.138]

Schdllkopfs chiral glycine enolate equivalents, as in the elegant synthesis of the central diarylether unit of ristocetin [169]. It is remarkable that these limitations were partly lifted by using, instead of the manganese tricarbonyl complex the corresponding iron or ruthenium cyclopentadienyl complexes [170] (Scheme 62). [Pg.311]

Electrochemical methods may be successfully utilized for the preparation of both mono- and poly-cyclopentadienyl complexes of many transition metals. During the dissolution of manganese at the anode in DMF which contains methylcyclopentadiene in the atmosphere of carbon monoxide, (methylcyclopentadienyl)tricarbonylmangenese is obtained ... [Pg.537]

Table 9.12, Properties of Manganese Group Cyclopentadienyl Complexes... Table 9.12, Properties of Manganese Group Cyclopentadienyl Complexes...
Many 7i-cyclopentadienyl complexes may be prepared from the reaction of alkali metal cyclopentadienides with ammonia-soluble transition metal salts such as nitrates and thiocyanates in liquid ammonia (2-30). The amine complexes, [M(NH3) ] (C5H5)2, lose ammonia when heated in vacuo, and the uncharged dicyclopentadienyl complexes of iron, cobalt, nickel, chromium, and manganese are obtained. [Pg.24]

The 1,2-oxaborolide anion (Figure 1), an analog of furan, has been prepared by two different routes and sandwich complexes with ruthenium and manganese 136, 137 have been characterized.153 Comparison of IR stretching frequencies suggests that oxaborolide is a weaker electron donor and better electron acceptor than cyclopentadienyl. [Pg.44]

In a similar manner, Jt-allyl complexes of manganese, iron, and molybdenum carbonyls have been obtained from the corresponding metal carbonyl halides [5], In the case of the reaction of dicarbonyl(r 5-cyclopentadienyl)molybdenum bromide with allyl bromide, the c-allyl derivative is obtained in 75% yield in dichloromethane, but the Jt-allyl complex is the sole product (95%), when the reaction is conducted in a watenbenzene two-phase system. Similar solvent effects are observed in the corresponding reaction of the iron compound. As with the cobalt tetracarbonyl anion, it is... [Pg.365]

The first metal-olefin complex was reported in 1827 by Zeise, but, until a few years ago, only palladium(II), platinum(Il), copper(I), silver(I), and mercury(II) were known to form such complexes (67, 188) and the nature of the bonding was not satisfactorily explained until 1951. However, recent work has shown that complexes of unsaturated hydrocarbons with metals of the vanadium, chromium, manganese, iron, and cobalt subgroups can be prepared when the metals are stabilized in a low-valent state by ligands such as carbon monoxide and the cyclopentadienyl anion. The wide variety of hydrocarbons which form complexes includes olefins, conjugated and nonconjugated polyolefins, cyclic polyolefins, and acetylenes. [Pg.78]

F,SCH, Methanesulfonic acid, trifluoro-iridium, manganese and rhenium complexes, 26 114, 115, 120 platinum complex, 26 126 OiFeCgH, Iron, acetyl dicarbonyl (if -cyclopentadienyl)-, 26 239 0,FeN2C2 Hll(, Iron, tricarbonylbis(2-isocy-ano-l,3-dimethylbenzene)-, 26 54 0.iMoNaCHH5-2 C4H ,02, Molybdate 1 -), tricarbonyl(T) -cyclopentadienyl)-sodium, compd. with 1,2-dimethoxy-ethane-(l 2), 26 343 0,NaWC H5-2 C4H ,02, Tungstate(l -), tricarbonyl(ris-cyclopentadienyl)-... [Pg.430]


See other pages where Manganese complexes cyclopentadienyl is mentioned: [Pg.297]    [Pg.189]    [Pg.191]    [Pg.196]    [Pg.100]    [Pg.122]    [Pg.138]    [Pg.286]    [Pg.565]    [Pg.55]    [Pg.234]    [Pg.729]    [Pg.443]    [Pg.357]    [Pg.427]    [Pg.119]    [Pg.158]    [Pg.218]    [Pg.345]    [Pg.436]    [Pg.19]    [Pg.31]    [Pg.240]    [Pg.170]    [Pg.195]    [Pg.95]    [Pg.436]    [Pg.131]    [Pg.44]   
See also in sourсe #XX -- [ Pg.19 , Pg.188 , Pg.196 ]

See also in sourсe #XX -- [ Pg.19 , Pg.188 , Pg.196 ]




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Complexes cyclopentadienyls

Cyclopentadienyl complex

Cyclopentadienyl complexe

Manganese complexes

Manganese complexing

Manganese cyclopentadienyl

Manganese cyclopentadienyls

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