Effect of axial anthracene ligands on the luminescence of trinickel molecular wires |
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| Authors: | F. Albert Cotton Hui Chao Zhong Li Carlos A. Murillo Qingsheng Wang |
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| Affiliation: | 1. Department of Chemistry, Laboratory for Molecular Structure and Bonding, P.O. Box 30012, Texas A&M University, College Station, TX 77842-3012, USA;2. School of Chemistry & Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, PR China;1. Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC 29208, USA;2. Department of Chemistry, Texas A&M University, College Station, TX 77843, USA;3. Department of Chemistry, Purdue University, West Lafayette, IN 47907, USA |
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| Abstract: | Two nickel compounds having extended metal atom chains (EMACs) with the Ni3(dpa)4L2 core, where dpa is the anion of 2,2′-dipyridylamine and L represents an anthracene derivative, have been synthesized in good yield and excellent purity by reaction of Ni3(dpa)4Cl2 and the respective anthracene derivatives. For the compound Ni3(dpa)4(AnCC)2 (1) AnCC is the anion of 9-ethynylanthracene and for Ni3(dpa)4(AnCOO)2 (2) AnCOO is anthracene-9-carboxylate. The two compounds have been characterized by X-ray crystallography and other techniques. The cyclovoltammograms (CVs) of 1 and 2 display reversible redox processes at E1/2 = 0.911 V and 1.020 V, respectively (vs. Ag/AgCl). The magnetic data suggest that the terminal Ni atoms are in a high spin state while the central Ni atom is diamagnetic, in agreement with other trinickel molecular wires. Although compound 1 is strongly luminescent, and represents the first such example in an EMAC, 2 does not display luminescence. The strong emission in 1 is related to donor–acceptor interactions between the Ni?Ni?Ni wire, the triply bonded C C linking unit, and the conjugated aromatic anthracene derivative, a process that is unavailable for 2 because the carboxylate group is almost perpendicular to the anthracene moiety. |
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