scholarly journals Dimethyloxonium and Methoxy Derivatives of nido-Carborane and Metal Complexes Thereof

Inorganics ◽  
2019 ◽  
Vol 7 (4) ◽  
pp. 46 ◽  
Author(s):  
Marina Yu. Stogniy ◽  
Svetlana A. Erokhina ◽  
Irina D. Kosenko ◽  
Andrey A. Semioshkin ◽  
Igor B. Sivaev

9-Dimethyloxonium, 10-dimethyloxonium, 9-methoxy and 10-methoxy derivatives of nido-carborane (9-Me2O-7,8-C2B9H11, 10-Me2O-7,8-C2B9H11, [9-MeO-7,8-C2B9H11]−, and [10-MeO-7,8-C2B9H11]−, respectively) were prepared by the reaction of the parent nido-carborane [7,8-C2B9H12]− with mercury(II) chloride in a mixture of benzene and dimethoxymethane. Reactions of the 9 and 10-dimethyloxonium derivatives with triethylamine, pyridine, and 3-methyl-6-nitro-1H-indazole result in their N-methylation with the formation of the corresponding salts with 9 and 10-methoxy-nido-carborane anions. The reaction of the symmetrical methoxy derivative [10-MeO-7,8-C2B9H11]− with anhydrous FeCl2 in tetrahydrofuran in the presence of t-BuOK results in the corresponding paramagnetic iron bis(dicarbollide) complex [8,8′-(MeO)2-3,3′-Fe(1,2-C2B9H10)2]−, whereas the similar reactions of the asymmetrical methoxy derivative [9-MeO-7,8-C2B9H11]− with FeCl2 and CoCl2 presumably produce the 4,7′-isomers [4,7′-(MeO)2-3,3′-M(1,2-C2B9H10)2]− (M = Fe, Co) rather than a mixture of rac-4,7′- and meso-4,4′-isomers.

1982 ◽  
Vol 47 (5) ◽  
pp. 1382-1391 ◽  
Author(s):  
Jiří Jílek ◽  
Josef Pomykáček ◽  
Jiřina Metyšová ◽  
Miroslav Protiva

Acids IIa-c were prepared by reactions of (4-fluoro-2-iodophenyl)acetic acid with 4-methoxythiophenol, 4-ethoxythiophenol and 4-(ethylthio)thiophenol and cyclized with polyphosphoric acid in boiling toluene to dibenzo[b,f]thiepin-10(11H)-ones IIIa-c. Reduction with sodium borohydride afforded the alcohols IVa-c which were treated with hydrogen chloride and gave the chloro derivatives Va-c. Substitution reactions with 1-methylpiperazine resulted in the title compounds Ia-c out of which the methoxy derivative Ia was transformed by demethylation with boron tribromide to the phenol Id. Compounds Ia-d are very potent neuroleptics exhibiting a clear prolongation of the central depressant and some prolongation of the cataleptic activity.


Chemistry ◽  
2021 ◽  
Vol 3 (1) ◽  
pp. 199-227
Author(s):  
Young Hoon Lee ◽  
Jee Young Kim ◽  
Sotaro Kusumoto ◽  
Hitomi Ohmagari ◽  
Miki Hasegawa ◽  
...  

Analysis of the weak interactions within the crystal structures of 33 complexes of various 4′-aromatic derivatives of 2,2′:6′,2″-terpyridine (tpy) shows that interactions that exceed dispersion are dominated, as expected, by cation⋯anion contacts but are associated with both ligand–ligand and ligand–solvent contacts, sometimes multicentred, in generally complicated arrays, probably largely determined by dispersion interactions between stacked aromatic units. With V(V) as the coordinating cation, there is evidence that the polarisation of the ligand results in an interaction exceeding dispersion at a carbon bound to nitrogen with oxygen or fluorine, an interaction unseen in the structures of M(II) (M = Fe, Co, Ni, Cu, Zn, Ru and Cd) complexes, except when 1,2,3-trimethoxyphenyl substituents are present in the 4′-tpy.


Molecules ◽  
2021 ◽  
Vol 26 (1) ◽  
pp. 210
Author(s):  
Alexander D. Ryabov

Reactions of cyclometalated compounds are numerous. This account is focused on one of such reactions, the exchange of cyclometalated ligands, a reaction between a cyclometalated compound and an incoming ligand that replaces a previously cyclometalated ligand to form a new metalacycle: + H-C*~Z ⇄ + H-C~Y. Originally discovered for PdII complexes with Y/Z = N, P, S, the exchange appeared to be a mechanistically challenging, simple, and convenient routine for the synthesis of cyclopalladated complexes. Over four decades it was expanded to cyclometalated derivatives of platinum, ruthenium, manganese, rhodium, and iridium. The exchange, which is also questionably referred to as transcyclometalation, offers attractive synthetic possibilities and assists in disclosing key mechanistic pathways associated with the C–H bond activation by transition metal complexes and C–M bond cleavage. Both synthetic and mechanistic aspects of the exchange are reviewed and discussed.


2019 ◽  
Vol 16 (31) ◽  
pp. 147-155
Author(s):  
Esmira A GULIYEVA ◽  
Zaur H GURBANOV ◽  
Yadigar A JABIYEV ◽  
Fikret SHEKILIYEV ◽  
Gulmamed Z SULEIMANOV ◽  
...  

The results of the development of synthesis technique of cyclocarbinol derivatives of cymantrene and the production of relevant barium cyclocarbinolate metal complexes – new, advanced anti-smoke additives were presented. Comparative data on the anti-smoke effectiveness of synthesized compounds and known antismoke additives for diesel fuels were also presented. Established, results of the development of a single-stage synthesis method of cyclocarbinol derivatives of cymantrene can be assumed as a basic process for producing high-effective anti-smoke additives to diesel fuels that comply with the requirements of ecology in operation of diesel vehicles.


1971 ◽  
Vol 24 (11) ◽  
pp. 2325 ◽  
Author(s):  
PJ Collin ◽  
WHF Sasse

Fourteen derivatives of the naphthalene-diphenylacetylene photo-adduct (1a) have been thermally isomerized to give high yields of derivatives of 1,2-diphenyl-2a,8b-dihydrocyclobuta[a]naphthalene (1b). Of these only the 4-methoxy derivative (13b) could be rearranged to the isomeric benzocyclooctatetraene (13c). Five alkyl and one methoxy derivative of (1b) were quantitatively isomerized to derivatives of (1a) but the isomerization of the esters (10b) and (11b) gave mixtures. Photo-iso- merization of the methoxybenzocyclooctatetraene (13c) gave exclusively (13b) and (13a). ��� Mechanistic aspects of these reactions are discussed.


Polyhedron ◽  
1995 ◽  
Vol 14 (10) ◽  
pp. 1397-1399 ◽  
Author(s):  
Nicanor Gálvez ◽  
Marcial Moreno-Mañas ◽  
Imma Padrós ◽  
Rosa Ma Sebastián ◽  
Neus Serra ◽  
...  

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