Heterobi- and -trinuclear Complexes with an Amino(ethynyl)carbene as Bridging Ligand

2004 ◽  
Vol 630 (12) ◽  
pp. 1863-1868 ◽  
Author(s):  
Helmut Fischer ◽  
Cornelia Hartbaum ◽  
Christiane Wespel ◽  
Markus Dede
1983 ◽  
Vol 22 (16) ◽  
pp. 2223-2224 ◽  
Author(s):  
Rosalvina R. Guimerans ◽  
Marilyn M. Olmstead ◽  
Alan L. Balch

1997 ◽  
Vol 36 (16) ◽  
pp. 3447-3454 ◽  
Author(s):  
Vǎn Ân Ung ◽  
Alexander M. W. Cargill Thompson ◽  
David A. Bardwell ◽  
Dante Gatteschi ◽  
John C. Jeffery ◽  
...  

Nanomaterials ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 3101
Author(s):  
Kiyoshi Fujisawa ◽  
Mai Saotome ◽  
Yoko Ishikawa ◽  
David James Young

Cyclic trinuclear complexes with group 11 metal (I) ions are fascinating and important to coordination chemistry. One of the ligands known to form these cyclic trinuclear complexes is pyrazolate, which is a bridging ligand that coordinates many transition metal ions in a Npz–M–Npz linear mode (Npz = pyrazolyl nitrogen atom). In these group 11 metal (I) ions, copper is the most abundant metal. Therefore, polynuclear Copper(I) complexes are very important in this field. The cyclic trinuclear Copper(I) complex [Cu(3,5-Ph2pz)]3 (3,5-Ph2pz– = 3,5-diphenyl-1-pyrazolate anion) was reported in 1988 as a landmark complex, but its photoluminescence properties have hitherto not been described. In this study, we report the photoluminescence and two different polymorphs of [Cu(3,5-Ph2pz)]3 and its derivative [Cu(3-Me-5-Phpz)]3 (3-Me-5-Phpz– = 3-metyl-5-phenyl-1-pyrazale anion). The substituents in [Cu(3-Me-5-Phpz)]3 cause smaller distortions in the solid-state structure and a red-shift in photoluminescence due to the presence of intermolecular cuprophilic interactions.


2008 ◽  
Vol 2 (2) ◽  
pp. 122-139
Author(s):  
Takashi Komiyama ◽  
Satoshi Igarashi ◽  
Yasuhiko Yukawa

2021 ◽  
Vol 60 (3) ◽  
pp. 1806-1813
Author(s):  
Husain N. Kagalwala ◽  
Mahesh S. Deshmukh ◽  
Elamparuthi Ramasamy ◽  
Neelima Nair ◽  
Rongwei Zhou ◽  
...  

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