Martí Marcelo A, Bari Sara E, Estrin Darío A, Doctorovich Fabio
Departamento de Química Inorgánica, Analítica y Qca. Física/INQUIMAE-CONICET, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pab II, P. 3, Buenos Aires (C1428EHA), Argentina.
J Am Chem Soc. 2005 Apr 6;127(13):4680-4. doi: 10.1021/ja044632n.
The water-soluble manganese(III) meso-tetrakis (N-ethylpyridinium-2-yl) porphyrin (Mn(III)TEPyP) and manganese(III) meso-(tetrakis(4-sulfonato-phenyl)) porphyrinate (Mn(III)TPPS) are able to chemically distinguish between HNO and NO donors, reacting with the former in a fast, efficient, and selective manner with concomitant formation of the {MnNO}(7) complex (k(on(HNO)) approximately equal to 10(5) M(-1) s(-1)), while they are inert or react very slowly with NO donors. DFT calculations and kinetic data suggest that HNO trapping is operative at least in the case of Mn(III)TPPS, while catalytic decomposition of the HNO donors (sodium trioxodinitrate and toluene sulfohydroxamic acid) seems to be the main pathway for Mn(III)TEPyP. In the presence of oxygen, the product Mn(II)TEPyP(NO) oxidizes back to Mn(III)TEPyP, making it possible to process large ratios of nitroxyl donor with small amounts of porphyrin.
水溶性的中-四(N-乙基吡啶-2-基)卟啉锰(III)(Mn(III)TEPyP)和中-(四(4-磺酸苯基))卟啉锰(III)(Mn(III)TPPS)能够在化学上区分HNO和NO供体,它们与前者以快速、高效且选择性的方式反应,同时形成{MnNO}(7)配合物(k(on(HNO))约等于10(5) M(-1) s(-1)),而它们对NO供体呈惰性或反应非常缓慢。密度泛函理论计算和动力学数据表明,至少在Mn(III)TPPS的情况下,HNO捕获起作用,而HNO供体(三氧二硝酸钠和甲苯磺基异羟肟酸)的催化分解似乎是Mn(III)TEPyP的主要途径。在有氧气存在的情况下,产物Mn(II)TEPyP(NO)会氧化回Mn(III)TEPyP,这使得用少量卟啉处理大量硝酰基供体成为可能。