Spectroscopic investigation on porphyrins nano-assemblies onto gold nanorods

被引:14
|
作者
Trapani, Mariachiara [1 ]
De Luca, Giovanna [2 ,3 ,4 ]
Romeo, Andrea [1 ,2 ,3 ]
Castriciano, Maria Angela [1 ]
Scolaro, Luigi Monsu [1 ,2 ,3 ]
机构
[1] Univ Messina, Dipartimento Sci Chim Biol Farmaceut & Ambientali, CNR, ISMN, Vle F Stagno DAlcontres 31, I-98166 Messina, Italy
[2] Univ Messina, Dipartimento Sci Chim Biol Farmaceut & Ambientali, Vle F Stagno DAlcontres 31, I-98166 Messina, Italy
[3] CIRCMSB, Vle F Stagno DAlcontres 31, I-98166 Messina, Italy
[4] CNR, IPCB, Ple Enrico Fermi 1, I-80055 Portici, NA, Italy
关键词
Gold nanorods; Porphyrin; Aggregation; Spectroscopic characterization; AU NANORODS; OPTICAL-PROPERTIES; FACILE SYNTHESIS; AGGREGATION; NANOPARTICLES; SIZE; TETRAKIS(4-SULFONATOPHENYL)PORPHYRIN; NANOCRYSTALS; CHEMISTRY; MICELLES;
D O I
10.1016/j.saa.2016.09.025
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The interaction between gold nanorods (Au NRs), synthesized by a conventional seeded growth protocol, and the anionic tetrakis-(4-sulfonatophenyl)porphyrin (TPPS4) has been investigated through various spectroscopic techniques. At neutral pH, the formation of H-aggregates and the inclusion of porphyrin monomers in CTAB micelles covering the nanorods have been evidenced. Under mild acidic conditions (pH = 3) a nano-hybrid assembly of porphyrin J-aggregates and Au NRs has been revealed. For the sake of comparison, Cu(II) and Zn(II) metal porphyrin derivatives as well as a cationic porphyrin have been studied in the same experimental conditions, showing that: i) CuTPPS4 forms porphyrin H-dimers onto the Au NRs; ii) ZnTPPS4 undergoes to demetallation, followed by acidification of the central core and eventually aggregation onto Au NRs; iii) cationic porphyrin does not interact with Au NRs. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:343 / 349
页数:7
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