Turner Mark, Vaughan Owain P H, Kyriakou Georgios, Watson David J, Scherer Lukas J, Davidson Greg J E, Sanders Jeremy K M, Lambert Richard M
Department of Chemistry, University of Cambridge, Cambridge CB2 1EW, United Kingdom.
J Am Chem Soc. 2009 Feb 11;131(5):1910-4. doi: 10.1021/ja8076389.
The adsorption and subsequent thermal chemistry of the acetyl-protected manganese porphyrin, SAcP-Mn(III)Cl on Ag(100) have been studied by high resolution XPS and temperature-programmed desorption. The deprotection event, leading to formation of the covalently bound thioporphyrin, has been characterized and the conditions necessary for removal of the axial chlorine ligand have been determined, thus establishing a methodology for creating tethered activated species that could serve as catalytic sites for delicate oxidation reactions. Surface-mediated acetyl deprotection occurs at 298 K, at which temperature porphyrin diffusion is limited. At temperatures above approximately 425 K porphyrin desorption, diffusion and deprotection occur and at >470 K the axial chlorine is removed.
通过高分辨率X射线光电子能谱(XPS)和程序升温脱附法,研究了乙酰基保护的锰卟啉SAcP-Mn(III)Cl在Ag(100)上的吸附及后续热化学过程。对导致共价键合硫卟啉形成的脱保护事件进行了表征,并确定了去除轴向氯配体所需的条件,从而建立了一种制备可作为精细氧化反应催化位点的 tethered 活化物种的方法。表面介导的乙酰基脱保护在298 K发生,此温度下卟啉扩散受限。在约425 K以上的温度,卟啉发生脱附、扩散和脱保护,且在>470 K时轴向氯被去除。