卟啉
三环己基膦
化学
磷化氢
叠氮化物
结晶学
金化合物
溶解
金团
无机化学
密度泛函理论
光化学
计算化学
物理化学
有机化学
组合化学
催化作用
作者
D.V. Partyka,Thomas J. Robilotto,Matthias Zeller,A.D. Hunter,Thomas Gray
标识
DOI:10.1073/pnas.0806520105
摘要
A silver- and Brönsted acid-free protocol for generating the (tricyclohexylphosphine)gold(I) cation from the corresponding azide complexes is disclosed. The gold(I) cations so liberated are trapped by complexation with octaethylporphyrin. The first structurally authenticated gold(I) porphyrin complex crystallizes with formula C 72 H 112 Au 2 F 12 N 4 P 2 Sb 2 , space group C 2/ c , a = 21.388 (4), b = 19.679 (4), c = 19.231 (3) Å; β = 111.030 (3)°. Solution spectroscopic studies indicate that the di-gold complex fragments on dissolution in organic solvents. Approximate density-functional theory calculations find an electrostatic origin for the binding of two gold(I) centers to the unprotonated nitrogen atoms, despite greater orbital density on the porphyrin meso carbons.
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