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Development of a nanoscale-based optical chemical sensor for the detection of NO radical
摘要： Nitric oxide is one of the most important biochemical parameters in biological processes; it is also known as carcinogenic. There is need for the design of stable and durable solid phase nitric oxide sensors. In this study, we immobilized the nitric oxide sensitive molecules pyrene, tris(2,2’-bipyrdyl)dichlororuthenium(II) hexahydrate (Ru(bipy) 2+ 3 ) , and magnesium phthalocyanine (Mg-Pc) for the first time in polymeric or glassy matrices. We applied silver nanoparticles and ionic liquids in the fabrication process of polymeric electrospun fibers and thin films. We compared their NO sensitivity in micelle solutions that mimic the cell medium by both steady state and lifetime-based fluorescence measurements. Among the tested dyes, the pyrene exhibited the highest response for radicalic NO. The Mg-Pc dye followed pyrene in terms of sensitivity and exhibited increasing fluorescence intensity and lifetime-based response. Lifetime-based response is advantageous and selective as it is not affected by source variations, photo-bleaching, or leaching effects. Another advantage of Mg-Pc dye is that it is not poisonous for organic systems. Presence of the ionic liquid enhanced the sensor response in all of the test moieties. The obtained limit of detection values for pyrene, Ru(bipy) 2+ and Mg-Pc dyes were 0.15 (cid:22) M, 1.54 (cid:22) M, and 0.78 (cid:22) M, respectively.
关键词： electrospinning,Nitric oxide radical,nanomaterials,ruthenium complex,magnesium phthalocyanine,pyrene,time resolved fluorescence
更新于2025-09-04 15:30:14
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Phthalocyanine Zinc‐catalyzed Hydroxylation of Aryl Boronic Acids under visible Light
摘要： A visible-light-promoted aerobic oxidative hydroxylation of boronic acids using phthalocyanine zinc as an easily available photosensitizer has been developed. It provided a direct access to synthesize aliphatic alcohols and phenols from boronic acids. The advantages of this approach included the low catalyst loading (0.5 mol %), high efficient, the use of O2 as an oxygen source, wide substrate range, the simple operational process, and mild conditions.
关键词： phenols,phthalocyanine zinc,visible light,boronic acids,aerobic oxidative hydroxylation
更新于2025-09-04 15:30:14
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Group 10 metal–thiocatecholate capped magnesium phthalocyanines – coupling chromophore and electron donor/acceptor entities and its impact on sulfur induced red-shifts
摘要： A new and facile method of generating thiolate groups at the phthalocyanine (Pc) β-position is presented as well the unique properties that these groups confer on the Pc ligand upon coordination of group 10 metals Ni, Pd and Pt(dppe) or SnMe3. In particular, the Q-band is shifted to almost 800 nm for all group 10 metals used, and the complexes show panchromatic absorption owing to new absorbance bands that appear between 400 and 650 nm. Enhanced intersystem-crossing for all transition metal co-ordinated Mg(Pc) complexes was demonstrated by the moderate to very high singlet oxygen quantum yields of 0.36, 0.76 and 0.91 for the Ni, Pd and Pt coordinating complexes, respectively, which show that the heavy metals have direct influence on the Pc π-system and inter-system-crossing (ISC). This was further confirmed by MO calculations, which show mixing of metal and ligand orbitals, as well as suggest that the Q-band transition has both π → π* and ligand-to-metal charge transfer characteristics. Furthermore, the origin of the Q-band red-shift was shown to be due to greater destabilization of the HOMO compared to LUMO/LUMO+1, thus decreasing the HOMO–LUMO band gap.
关键词： thiolate groups,intersystem-crossing,phthalocyanine,MO calculations,HOMO–LUMO band gap,panchromatic absorption,singlet oxygen quantum yields,group 10 metals,Q-band
更新于2025-09-04 15:30:14