Design of an NO photoinduced releaser xerogel based on the controlled nitric oxide donor trans-[Ru(NO)Cl(cyclam)](PF6)2 (cyclam=1,4,8, 11-tetraazacyclotetradecane)

被引:28
作者
Ferreira, Kleber Queiroz
Schneider, Jose F.
Nascente, Pedro A. P.
Rodrigues-Filho, Ubirajara Pereira
Tfouni, Elia
机构
[1] Univ Sao Paulo, Fac Filosofia Ciencias & Letras Ribeirao Preto, Dept Quim, BR-14040901 Ribeirao Preto, Brazil
[2] Univ Sao Paulo, Inst Fis Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
[3] Univ Fed Sao Carlos, Dept Engn Mat, BR-13565905 Sao Carlos, SP, Brazil
[4] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13560970 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
nitric oxide; sol-gel; xerogel; ruthenium; nitrosyl; controlled; photochemistry; cyclam; silica; aminopropylsilica; nucleophilic; attack;
D O I
10.1016/j.jcis.2006.03.081
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The immobilization and properties of the nitric oxide donor trans-[Ru(NO)Cl(cyclam)](PF6)(2), Ru-NO, entrapped in a silica matrix by the solGel process is reported herein. The entrapped nitrosyl complex was characterized by spectroscopic (UV-vis, infrared (IR), X-ray photoelectron, and C-13 and Si-29 MAS NMR) and electrochemical techniques. The entrapped species exhibit one characteristic absorption band in the UV-vis region of the electronic spectrum at 354 nm and one IR v(NO) stretching band at 1865 cm(-1), as does the Ru-NO species in aqueous solution. Our results show that trans-[Ru(NO)Cl(cyclam)](PF6)(2) can be entrapped in a SiO2 matrix with preservation of the molecular structure. However, in a SiO2/SiNH2 matrix, the complex undergoes a nucleophilic attack by the amine group at the nitrosonium. Irradiation of the complex, entrapped in the SiO2 matrix, with light of 334 nm, resulted in NO release. The material was regenerated to its initial nitrosyl form by reaction with nitric oxide. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:543 / 552
页数:10
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