The Visible Spectra and Electronic Effects in Axial Coordination Reaction of Zinc Porphyrin Complexes

1997 ◽  
Vol 13 (07) ◽  
pp. 603-611
Author(s):  
Ruan Wen-Juan ◽  
◽  
Zhu Zhi-Ang ◽  
Chen Hong-Wei ◽  
Bu Xian-He ◽  
...  
2021 ◽  
Author(s):  
Ryo Sasai ◽  
Yu-hei Aoyama ◽  
Takuya Fujimura

Abstract In this study, we investigated the axial coordination reaction between pyridine and zinc meso-tetra(4-sulfonatophenyl)porphyrin (ZnTPPS) incorporated in a transparent layered double hydroxide (LDH) film modified with 1-decanesulfonate (C10S) in an aqueous solution. The equilibrium constant (\({K}_{11}\)) of the axial coordination reaction between pyridine and ZnTPPS incorporated in the transparent ZnTPPS/C10S/LDH film was approximately 260 times that of the corresponding reaction in an aqueous solution. The hydrophobisation of the LDH interlayer space by C10S, which led to the elimination of water molecules surrounding ZnTPPS and enabled the accumulation of pyridine molecules, was responsible for such a significant increase in the \({K}_{11}\) value. The developed film can detect pyridine in aqueous solutions with ultra-high sensitivity in the order of 10−5 mol/L through changes in the colour tone, which is comparable to the molecular detection ability of insect antennae. The sensing response was also observed at pyridine concentrations as low as 10−9 mol/L.


2021 ◽  
Author(s):  
Ryo Sasai ◽  
Yu-hei Aoyama ◽  
Takuya Fujimura

Abstract In this study, we investigated the axial coordination reaction between pyridine and zinc meso-tetra(4-sulfonatophenyl)porphyrin (ZnTPPS) incorporated in a transparent layered double hydroxide (LDH) film modified with 1-decanesulfonate (C10S) in an aqueous solution. The equilibrium constant (K11) of the axial coordination reaction between pyridine and ZnTPPS incorporated in the transparent ZnTPPS/C10S/LDH film was approximately 260 times that of the corresponding reaction in an aqueous solution. The hydrophobisation of the LDH interlayer space by C10S, which led to the elimination of water molecules surrounding ZnTPPS and enabled the accumulation of pyridine molecules, was responsible for such a significant increase in the K11 value. The developed film can detect pyridine in aqueous solutions with ultra-high sensitivity in the order of 10−5 mol/L through changes in the colour tone, which is comparable to the molecular detection ability of insect antennae. The sensing response was also observed at pyridine concentrations as low as 10−9 mol/L.


2010 ◽  
Vol 17 (5) ◽  
pp. 438-447 ◽  
Author(s):  
Wen-Juan Ruan ◽  
Zhi-Ang Zhu ◽  
Xian-He Bu ◽  
Zhi-Hui Zhang ◽  
Yun-Ti Chen

1999 ◽  
Vol 15 (02) ◽  
pp. 167-172
Author(s):  
Feng Hai-Xia ◽  
◽  
Zhu Zhi-Ang ◽  
Wang Chuan-Zhong ◽  
Ruan Wen-Juan ◽  
...  

2010 ◽  
Vol 14 (03) ◽  
pp. 235-243 ◽  
Author(s):  
Baojiao Gao ◽  
Ruixin Wang ◽  
Ruikui Du

Cobalt tetra(para-chlorophenyl)porphyrin ( CoTCPP ) and zinc tetraphenyl porphyrin ( ZnTPP ) were linked on the side chains of the copolymer of 4-vinylpyridine (4VP) and styrene (St), P(4VP-co-St), via axial coordination reactions, respectively, and the metalloporphyrin-functionalized macromolecules, CoTCPP -P(4VP-co-St) and ZnTPP -P(4VP-co-St), were prepared. Their chemical structures were characterized by FTIR and 1H NMR. The spectral properties of the two macromolecular axial coordination complexes were mainly studied, and their photophysical behavior were discussed in depth. The experimental results show that the metalloporphyrin-functionalized macromolecules, CoTCPP -P(4VP-co-St) and ZnTPP -P(4VP-co-St), can be prepared favorably through axial coordination reaction with the side pyridine groups of the copolymer P(4VP-co-St) as ligands. The two complexes have characteristic spectra similar to that of the small molecular metalloporphyrins, CoTCPP and ZnTPP , respectively. At the same time, they also display the characteristic spectroscopic property of axial coordination complexes: the electronic adsorption spectra of CoTCPP -P(4VP-co-St) and ZnTPP -P(4VP-co-St) red-shifted obviously as compared to that of CoTCPP and ZnTPP , and the fluorescence emission of ZnTPP -P(4VP-co-St) blue-shifted apparently with respect to that of ZnTPP . For CoTCPP -P(4VP-co-St) and ZnTPP -P(4VP-co-St), some polymer effects were found: (1) the bonding degree of the small molecular metalloporphyrin, CoTCPP or ZnTPP , on the side chains of the copolymer P(4VP-co-St) has a limit value because of the steric hindrance and there is a bonding degree difference between the actual value and the theoretical value; (2) for ZnTPP -P(4VP-co-St), slight energy transfer between adjacent ZnTPP units on an identical macromolecule occurs, leading to slight static quench of the fluorescence emission as the bonding density of ZnTPP units on the side chains of the copolymer P(4VP-co-St) reaches a certain value.


2004 ◽  
Vol 108 (31) ◽  
pp. 11333-11343 ◽  
Author(s):  
Francis D'Souza ◽  
Phillip M. Smith ◽  
Suresh Gadde ◽  
Amy L. McCarty ◽  
Michael J. Kullman ◽  
...  

1997 ◽  
Vol 13 (09) ◽  
pp. 838-842
Author(s):  
Guo Fu-Chun ◽  
◽  
Chen De-Wen ◽  
Xu Guang-Zhi

2007 ◽  
Vol 121-123 ◽  
pp. 653-656 ◽  
Author(s):  
Y.W. Jin ◽  
W. Liu ◽  
Yi Yang Zhao ◽  
C. Wang

Functional self-assembled structure with well-defined shapes and dimensions are of great current interest. Porphyrins are attractive building manifold patterning for these structures because of their electronic, optical, and catalytic properties. In this paper, we report a novel technique for the assembly patterning of polymers. An Electrospinning process was used to create patterning with diameter ranging from 3 μm to 4 μm and length of up to several hundred micrometers in the presence of Zinc Porphyrin. Scanning electron microscopy (SEM), UV- visible spectra and EDX spectra were used to characterize the patterning. The results indicated that the patterning depended on the concentration of Porphyrin and the operational conditions.


2013 ◽  
Vol 575-576 ◽  
pp. 123-129
Author(s):  
Zhuang Dong Yuan ◽  
Jing Xia Wang ◽  
Ning Sheng

DABCO (1, 4-diazabicyclo [2.2.2] octane) has been used in combination with pentameric zinc porphyrin-pyrene array 1 to form well-defined supramolecular arrays through axial coordination. The self-assembly process has been investigated by a wide range of spectroscopic methods including UV-vis, fluorescence emission and 1H NMR techniques.


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