A Tris(diisocyanide)chromium(0) Complex Is a Luminescent Analog of Fe(2,2′-Bipyridine)32+

详细信息    查看全文

• 作者：Laura A. Büldt ; Xingwei Guo ; Raphael Vogel ; Alessandro Prescimone ; Oliver S. Wenger
• 刊名：Journal of the American Chemical Society
• 出版年：2017
• 出版时间：January 18, 2017
• 年：2017
• 卷：139
• 期：2
• 页码：985-992
• 全文大小：595K
• ISSN：1520-5126

文摘

A meta-terphenyl unit was substituted with an isocyanide group on each of its two terminal aryls to afford a bidentate chelating ligand (CN^tBuAr₃NC) that is able to stabilize chromium in its zerovalent oxidation state. The homoleptic Cr(CN^tBuAr₃NC)₃ complex luminesces in solution at room temperature, and its excited-state lifetime (2.2 ns in deaerated THF at 20 °C) is nearly 2 orders of magnitude longer than the current record lifetime for isoelectronic Fe(II) complexes, which are of significant interest as earth-abundant sensitizers in dye-sensitized solar cells. Due to its chelating ligands, Cr(CN^tBuAr₃NC)₃ is more robust than Cr(0) complexes with carbonyl or monodentate isocyanides, manifesting in comparatively slow photodegradation. In the presence of excess anthracene in solution, efficient energy transfer and subsequent triplet–triplet annihilation upconversion is observed. With an excited-state oxidation potential of −2.43 V vs Fc⁺/Fc, the Cr(0) complex is a very strong photoreductant. The findings presented herein are relevant for replacement of precious metals in dye-sensitized solar cells and in luminescent devices by earth-abundant elements.