scholarly journals Ultra-Sensitive Detection of Pyridine in Water Using Zinc Porphyrin Incorporated in a Transparent Hydrophobic Film

2021 ◽  
Author(s):  
Ryo Sasai ◽  
Yu-hei Aoyama ◽  
Takuya Fujimura
Keyword(s):  
Aqueous Solution ◽  
Molecular Detection ◽  
Interlayer Space ◽  
High Sensitivity ◽  
Water Molecules ◽  
Detection Ability ◽  
Zinc Porphyrin ◽  
Axial Coordination ◽  
Double Hydroxide ◽  
Coordination Reaction

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.

scholarly journals Ultra-Sensitive Detection of Pyridine in Water Using Zinc Porphyrin Incorporated in a Transparent Hydrophobic Film

2021 ◽  
Author(s):  
Ryo Sasai ◽  
Yu-hei Aoyama ◽  
Takuya Fujimura
Keyword(s):  
Aqueous Solution ◽  
Molecular Detection ◽  
Interlayer Space ◽  
High Sensitivity ◽  
Water Molecules ◽  
Detection Ability ◽  
Zinc Porphyrin ◽  
Axial Coordination ◽  
Double Hydroxide ◽  
Coordination Reaction

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.

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 ◽  
...  
Keyword(s):  
Electronic Effects ◽  
Zinc Porphyrin ◽  
Axial Coordination ◽  
Visible Spectra ◽  
Coordination Reaction

scholarly journals Ni/Cr-[α-SiW12O40] Layered Double Hydroxide as Effective Adsorbent of Iron(II) From Aqueous Solution

2021 ◽  
Vol 23 (2) ◽  
pp. 103
Author(s):  
A. Lesbani ◽  
M.F. Azmi ◽  
N.R. Palapa ◽  
T. Taher ◽  
R. Andreas ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Adsorption Capacity ◽  
Layered Double Hydroxide ◽  
Interlayer Space ◽  
Physical Adsorption ◽  
High Surface ◽  
High Surface Area ◽  
X Ray ◽  
Endothermic Process ◽  
Double Hydroxide

Layered double hydroxide (LDH) Ni/Cr intercalated [α-SiW12O40]4- has been prepared using the coprecipitation method. Materials were characterized by X-ray, FTIR, BET, and pHpzc analyses. Material Ni/Cr-[α-SiW12O40] LDHs exhibited a high surface area 98.986 m2 g-1 from 11.030 m2 g-1 for Ni/Cr LDH where the interlayer space was an increase from 7.99 to 10.87 Å with indicated that high crystallinity. Ni/Cr-[α-SiW12O40] LDHs showed higher adsorption capacity for iron(II) is up to 250 mg g-1. Adsorption of iron(II) on LDHs has an endothermic process and classify as physical adsorption.

Thermodynamic study of axial coordination reaction of zinc porphyrin with metal Schiff base and imidazole complex

2010 ◽  
Vol 17 (5) ◽  
pp. 438-447 ◽  
Author(s):  
Wen-Juan Ruan ◽  
Zhi-Ang Zhu ◽  
Xian-He Bu ◽  
Zhi-Hui Zhang ◽  
Yun-Ti Chen
Keyword(s):  
Schiff Base ◽  
Thermodynamic Study ◽  
Zinc Porphyrin ◽  
Axial Coordination ◽  
Coordination Reaction

Structural Study of a new Compound Based on Acid 1,4-Cyclohexanedicarboxylic (1,4-CDC)

2010 ◽  
Vol 6 (1) ◽  
pp. 891-896
Author(s):  
Manel Halouani ◽  
M. Dammak ◽  
N. Audebrand ◽  
L. Ktari
Keyword(s):  
Aqueous Solution ◽  
Water Molecules ◽  
Carboxyl Group ◽  
X Ray Diffraction ◽  
Compound I ◽  
Unit Cell Parameters ◽  
Monoclinic System ◽  
X Ray ◽  
Cell Parameters ◽  
Cyclohexanedicarboxylic Acid

One nickel 1,4-cyclohexanedicarboxylate coordination polymers, Ni2 [(O10C6H4)(COO)2].2H2O  (I), was hydrothermally synthesized from an aqueous solution of Ni (NO3)2.6H2O, (1,4-CDC) (1,4-CDC = 1,4-cyclohexanedicarboxylic acid) and tetramethylammonium nitrate. Compound (I) crystallizes in the monoclinic system with the C2/m space group. The unit cell parameters are a = 20.1160 (16) Å, b = 9.9387 (10) Å, c = 6.3672 (6) Å, β = 97.007 (3) (°), V= 1263.5 (2) (Å3) and Dx= 1.751g/cm3. The refinement converged into R= 0.036 and RW = 0.092. The structure, determined by single crystal X-ray diffraction, consists of two nickel atoms Ni (1) and Ni (2). Lots of ways of which is surrounded by six oxygen atoms, a carboxyl group and two water molecules.

scholarly journals Highly sensitive detection of nitrobenzene by a series of fluorescent 2D zinc(ii) metal–organic frameworks with a flexible triangular ligand

RSC Advances ◽  
2021 ◽  
Vol 11 (39) ◽  
pp. 23975-23984
Author(s):  
Xue Yang ◽  
Yixia Ren ◽  
Hongmei Chai ◽  
Xiufang Hou ◽  
Zhixiang Wang ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Metal Organic Frameworks ◽  
High Sensitivity ◽  
Fluorescent Sensors ◽  
Sensitive Detection ◽  
Donor Ligands ◽  
Highly Sensitive ◽  
Metal Organic ◽  
Highly Sensitive Detection

Four fluorescent 2D Zn-MOFs based on a flexible triangular ligand and linear N-donor ligands are hydrothermally prepared and used to detect nitrobenzene in aqueous solution with high sensitivity, demonstrating their potential as fluorescent sensors.

Investigation of layered double hydroxide/carbon dot nanocomposite on removal efficiency of Pb2+ from aqueous solution

2021 ◽  
pp. 116774
Author(s):  
Fataneh Vasheghani Farahani ◽  
Mohammad Hassan Amini ◽  
Seyed Hamid Ahmadi ◽  
Seyed Amirabbas Zakaria
Keyword(s):  
Aqueous Solution ◽  
Layered Double Hydroxide ◽  
Removal Efficiency ◽  
Carbon Dot ◽  
Double Hydroxide

Restricted Rotational Motion of InterlayerWaterMolecules in Vanadium Pentoxide Hydrate, V2O5·n D2O, as Studied by Deuterium NMR

2002 ◽  
Vol 57 (6-7) ◽  
pp. 419-424 ◽  
Author(s):  
Sadamu Takeda ◽  
Yuko Gotoh ◽  
Goro Maruta ◽  
Shuichi Takahara ◽  
Shigeharu Kittaka
Keyword(s):  
Double Layer ◽  
Vanadium Pentoxide ◽  
Rotational Motion ◽  
Interlayer Space ◽  
Layer Structure ◽  
Bond Distance ◽  
Adsorbed Water ◽  
Deuterium Nmr ◽  
Water Molecules ◽  
Layer Structures

The rotational behavior of the interlayer water molecules of deuterated vanadium pentoxide hydrate, V2O5.nD2O, was studied by solid-state deuterium NMR for the mono- and double-layer structures of the adsorbed water molecules. The rotational motion was anisotropic even at 355 K for both the mono- and double-layer structures. The 180° flipping motion about the C2-symmetry axis of the water molecule and the rotation around the figure axis, which makes an angle Ɵ with the C2-axis, occurred with the activation energy of (34±4) and (49±6) kJmol-1, respectively. The activation energies were almost independent of the mono- and double-layer structures of the water molecules, but the angle Ɵ made by the two axes varied from 33° for the monolayer to 25° for the double-layer at 230 K. The angle started to decrease above 250 K (e. g. the angle was 17 at 355 K for the double-layer structure). The results indicate that the average orientation of the water molecules in the two dimensional interlayer space depends on the layer structure and on the temperature. From the deuterium NMR spectrum at 130 K, the quadrupole coupling constant e2Qq/h = 240 kHz and the asymmetry parameter η= 0.12 were deduced. These values indicate the average hydrogen bond distance R(O H) = 2.0 Å for the D2O molecules in the 2D-interlayer space

Meso tetrakis ortho-, meta-, and para-N-alkylpyridiniopor-phyrins: kinetics of copper(II) and zinc(II) incorporation and zinc porphyrin demetalation

2003 ◽  
Vol 07 (03) ◽  
pp. 139-146 ◽  
Author(s):  
Peter Hambright ◽  
Ines Batinić-Haberle ◽  
Ivan Spasojević
Keyword(s):  
Aqueous Solution ◽  
Ionic Strength ◽  
Effective Charge ◽  
Methyl Ethyl ◽  
Ionic Strength Dependence ◽  
Zinc Porphyrin ◽  
Cationic Porphyrin ◽  
Strength Dependence ◽  
Acid Catalyzed ◽  
Kinetics Of

The relative reactivities of the tetrakis( N -alkylpyridinium- X - yl )-porphyrins where X = 4 (alkyl = methyl, ethyl, n -propyl) , X = 3 (methyl) , and X = 2 (methyl, ethyl, n -propyl, n -butyl, n -hexyl, n -octyl) were studied in aqueous solution. From the ionic strength dependence of the metalation rate constants, the effective charge of a particular cationic porphyrin was usually larger when copper(II) rather than zinc(II) was the reactant. The kinetics of ZnOH + incorporation and the acid catalyzed removal of zinc from the porphyrins in 1.0 M HCl were also studied. In general, the more basic 4- (para-) and 3- (meta-) isomers were the most reactive, followed by the less basic 2- (ortho-) methyl to n -butyl derivatives, with the lipophilic ortho n -hexyl and n -octyl porphyrins the least reactive.

Sign in / Sign up

Export Citation Format

Share Document