Oberflächenverbindungen von Übergangsmetallen, XXV [1]: Redoxreaktionen von Oberfläehen-Chrom(II) auf Silicagel mit Olefinen / Surface Compounds of Transition Metals, XXV [1]: Redox Reactions of Surface Chromium(II) on Silicagel with Olefins

1983 ◽  
Vol 38 (11) ◽  
pp. 1412-1418 ◽  
Author(s):  
Hans-Ludwig Krauss ◽  
Erich Hums

AbstractOlefins may react with chromium(II)/silicagel catalysts at temperatures from 100 to 600 °C under formation of C1-C4 n-alkanes and organometallic species; the chromium is oxidized simultaneously. By this reaction the catalytic sites loose the ability for olefin polymerization and 〈CH2〉 transfer. A following treatment of the catalyst with hydrogen at 400 °C produces a second crop of alkanes from former organometallic species under partial reduction of the chromium back to CrII ; the polymerization activity is restorted correspondingly.

Author(s):  
Martin Klussmann ◽  
Sensheng Liu

Transition metals are the dominant catalysts for redox-reactions between peroxides and organic substrates. Here, we show that triarylamines can act as organic redox-catalysts, enabling oxidative difunctionalization reactions of alkenes and...


Author(s):  
Jaewoon Lee ◽  
Sojung Koo ◽  
Jinwoo Lee ◽  
Duho Kim

Considering Mn4+ (3d3)-based cations, various layered oxides (A[AyM1-y]O2, where A and M refer to alkali metals and transition metals, respectively) exhibiting oxygen-redox reactions have been investigated extensively to achieve high...


1978 ◽  
Vol 33 (11) ◽  
pp. 1278-1284 ◽  
Author(s):  
Hans-Ludwig Krauss ◽  
Ulrich Westphal

Abstract Surface chromium(II) supported on silica forms 1:1 and 1:2 complexes with defines; polyenes prefer chelate structures. For the ligand-to-metal bond a “Zeise-Salt” type is postulated. Secondary reactions include cis-trans isomerisation, shift of double bond, rearrangement of C-framework and polymerization/oligomerization. Cyclopentadiene obviously gives a h5 -cyclopentadienyl/hydrogen complex by oxidative addition followed by H2 emission and formation of a h5 -cp-CrIII complex; in this case the metal can be split off from the support by H+ without cleavage of the cp-Cr-bond.


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