Molecular Wire Consisting of a C8Chain of Elemental Carbon Bridging Two Metal Centers:  Synthesis and Characterization of [{Fe(η5-C5Me5)(dppe)}2(μ-C8)]

1996 ◽  
Vol 15 (2) ◽  
pp. 477-479 ◽  
Author(s):  
Françoise Coat ◽  
Claude Lapinte
1995 ◽  
Vol 14 (10) ◽  
pp. 4559-4569 ◽  
Author(s):  
Saeed Attar ◽  
John H. Nelson ◽  
Jean Fischer ◽  
Andre de Cian ◽  
Jean-Pascal Sutter ◽  
...  

2000 ◽  
Vol 611 (1-2) ◽  
pp. 551-557 ◽  
Author(s):  
Takuji Ogawa ◽  
Hiroyuki Furuta ◽  
Minako Takahashi ◽  
Ayako Morino ◽  
Hidemitsu Uno

Reactions ◽  
2021 ◽  
Vol 2 (3) ◽  
pp. 323-332
Author(s):  
Luis G. Alves ◽  
Ana M. Martins

In this study, new mono- and di-alkoxido zirconium(IV) complexes supported by tetradentate dianionic cyclam ligands were synthesized and characterized. These compounds were obtained by reaction of the parent Zr(IV) dichlorido species with one or two equivalents of the corresponding lithium alkoxido, whereas (3,5-Me2Bn2Cyclam)Zr(OPh)2 was prepared by protonolysis of the orthometallated species (3,5-Me-C6H4CH2)2Cyclam)Zr with phenol. The solid-state molecular structures of (Bn2Cyclam)ZrCl(OtBu) and (4-tBuBn2Cyclam)Zr(OiPr)2 show a trigonal prismatic geometry around the metal centers. (Bn2Cyclam)Zr(SPh)(OtBu) and (Bn2Cyclam)ZrMe(OiPr) were prepared by reaction of (Bn2Cyclam)ZrCl(OR) (R = iPr, tBu) with one equivalent of LiSPh or MeMgCl, respectively. The reactions of (Bn2Cyclam)Zr(OiPr)2 and (4-tBuBn2Cyclam)Zr(OiPr)2 with carbon dioxide suggested the formation of species that correspond to the addition of four CO2 molecules.


1997 ◽  
Vol 119 (4) ◽  
pp. 756-760 ◽  
Author(s):  
Lawrence R. Sita ◽  
Rimo Xi ◽  
Glenn P. A. Yap ◽  
Louise M. Liable-Sands ◽  
Arnold L. Rheingold

2016 ◽  
Vol 55 (31) ◽  
pp. 8856-8859 ◽  
Author(s):  
Robert J. Woolfson ◽  
Grigore A. Timco ◽  
Alessandro Chiesa ◽  
Inigo J. Vitorica-Yrezabal ◽  
Floriana Tuna ◽  
...  

Molecules ◽  
2020 ◽  
Vol 25 (4) ◽  
pp. 855 ◽  
Author(s):  
Fabian Fürmeyer ◽  
Danny Münzberg ◽  
Luca M. Carrella ◽  
Eva Rentschler

Herein we report the synthesis and characterization of a novel bis-tridentate 1,3,4-thiadiazole ligand (L = 2,5-bis[(2-pyridylmethyl)thio]methyl-1,3,4-thiadiazole). Two new mononuclear complexes of the type [MII(L)2](ClO4)2 (with M = FeII (C1) and CoII (C2)) have been synthesized, containing the new ligand (L). In both complexes the metal centers are coordinated by an N4S2-donorset and each of the two ligands is donating to the metal ion with just one of the tridentate pockets. The iron(II) complex (C1) is in the low spin [LS] state below room temperature and shows an increase in the magnetic moment only above 300 K. In contrast, the cobalt(II) complex (C2) shows a gradual spin crossover (SCO) with T1/2 = 175 K. To our knowledge, this is the first cobalt(II) SCO complex with an N4S2-coordination.


2016 ◽  
Vol 128 (31) ◽  
pp. 9002-9005 ◽  
Author(s):  
Robert J. Woolfson ◽  
Grigore A. Timco ◽  
Alessandro Chiesa ◽  
Inigo J. Vitorica-Yrezabal ◽  
Floriana Tuna ◽  
...  

KIMIKA ◽  
2010 ◽  
Vol 23 ◽  
pp. 55-63
Author(s):  
Girlie Naomi N. Sison ◽  
Arnie R. De Leon ◽  
Janir T. Datukan

A number of transition metal complexes have been investigated as potential electrocatalystsfor C02 reduction. Among these are rhenium monometallic complexes, which have shownunique activity towards C02 reduction. Further development of multimetallic systems,capable of storing multiple equivalents of electrons has shown some potential in increasingthe selectivity of the C02 conversion processes toward highly reduced products. This studyreports the synthesis and characterization of novel polynuclear rhenium(I) complexes whererhenium is incorporated to the bridging ligand tppq (2,3,7,8-tetra-2-pyridylpyrazino[2,3-g]quinoxaline), which is capable of attaching up to four metal centers. The resultingcomplexes were characterized using different spectroscopic techniques (infrared, UV-Vis,emission) and cyclic voltammetry. The results suggest that the synthetic procedure adoptedwas successful.


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