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meso-Tetraphenylporphyrin-Ag(II) is an organometallic complex that features a porphyrin ring with four phenyl groups attached to it, along with an Ag(II) ion coordinated to the porphyrin ring. meso-Tetraphenylporphyrin-Ag(II) is known for its unique properties and reactivity, stemming from the combination of the porphyrin ring and the silver ion.

14641-64-6

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14641-64-6 Usage

Uses

Used in Catalysis:
meso-Tetraphenylporphyrin-Ag(II) is used as a catalyst in various chemical reactions due to its unique structure and reactivity. The silver ion's ability to participate in redox reactions and the porphyrin ring's light interaction properties make it a promising candidate for catalytic applications.
Used in Material Science:
In the field of material science, meso-Tetraphenylporphyrin-Ag(II) is utilized for the development of new materials with specific technological applications. Its structure and the reactivity of the silver ion contribute to the creation of innovative materials with tailored properties.
Used in Photochemistry:
meso-Tetraphenylporphyrin-Ag(II) is also used in photochemistry, where its interaction with light and ability to undergo redox reactions are of particular interest. This makes it a valuable compound for research and applications involving light-induced processes and reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 14641-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,4 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14641-64:
(7*1)+(6*4)+(5*6)+(4*4)+(3*1)+(2*6)+(1*4)=96
96 % 10 = 6
So 14641-64-6 is a valid CAS Registry Number.

14641-64-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name meso-tetraphenylporphyrinatosilver(II)

1.2 Other means of identification

Product number -
Other names MESO-TETRAPHENYLPORPHYRIN-AG(II)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14641-64-6 SDS

14641-64-6Relevant academic research and scientific papers

Structure and stability of H+ associates of (5,10,15,20- tetraphenylporphinato)silver(II) in trifluoroacetic acid

Bichan,Tyulyaeva,Lomova

, p. 1345 - 1350 (2014)

Direct experimental confirmation of the formation of ion-molecular associates of (5,10,15,20-tetraphenyl-21H,23H-porphinato)silver(II) (AgTPP) with solvent protons in CF3COOH is obtained by means of 1H NMR spectroscopy. Their structure and spectral properties, as well as the kinetics of dissociation on metal-nitrogen bonds, depending on the concentration of CF3COOH (89-100%) and temperature (298-328 K), are studied It is shown that AgTPP acts as a C-base during the formation of H+ associates, the coordination centers of which have a high stability.

Observations on the Mechanochemical Insertion of Zinc(II), Copper(II), Magnesium(II), and Select Other Metal(II) Ions into Porphyrins

Atoyebi, Adewole O.,Brückner, Christian

supporting information, p. 9631 - 9642 (2019/03/26)

Building on a proof of concept study that showed the possibility of the mechanochemical insertion of some M(II) metals into meso-tetraphenylporphyrin using a ball mill as an alternative to traditional solution-based methods, we present here a detailed study of the influence of the many experimental variables on the reaction outcome performed in a planetary mill. Using primarily the mechanochemical zinc, copper, and magnesium insertion reactions, the scope and limits of the type of porphyrins (electron-rich or electron-poor meso-tetraarylporphyrins, synthetic or naturally occurring octaalkylporphyrins, and meso-triphenylcorrole) and metal ion sources suitable for this metal insertion modality were determined. We demonstrate the influence of the experimental metal insertion parameters, such as ball mill speed and reaction time, and investigated the often surprising roles of a variety of grinding agents. Also, the mechanochemical reaction conditions that remove zinc from a zinc porphyrin complex or exchange it for copper were studied. Using some standardized conditions, we also screened the feasibility of a number of other metal(II) insertion reactions (VO, Ni, Fe, Co, Ag, Cd, Pd, Pt, Pb). The underlying factors determining the rates of the insertion reactions were found to be complex and not always readily predictable. Some findings of fundamental significance for the mechanistic understanding of the mechanochemical insertion of metal ions into porphyrins are highlighted. Particularly the mechanochemical insertion of Mg(II) is a mild alternative to established solution methods. The work provides a baseline from which the practitioner may start to evaluate the mechanochemical metal insertion into porphyrins using a planetary ball mill.

Synthesis of Ag(II) 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-Tetraphenylporphyrin and its facile demetalation to 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-Tetraphenylporphyrin

Ravindran, Sasitha Vidyarini,Pennathur, Anuj Krishnasundar,Nandhini Devi,Pennathur, Gautam

, p. 656 - 661 (2016/07/11)

A novel one-step strategy for the synthesis of 2,3,7,8,12,13,17,18-octabromo-5,10,15,20-Tetraphenylporphyrin using AgIIOBP is described. AgIIOBP was synthesized and was. Bromination of AgIITPP was carried out in a one-step reaction by varying the subseque

Dual facet of gold(iii) in the reactions of gold(iii) and porphyrins

Lv, Hongbin,Yang, Boyan,Jing, Jing,Yu, Yi,Zhang, Jing,Zhang, Jun-Long

supporting information; experimental part, p. 3116 - 3118 (2012/04/10)

We have firstly demonstrated the dual facet of gold(iii) in the reaction between gold(iii) and porphyrins, which could be tuned through changing the counter ions, ligands and the electronic effect of the substituents of the porphyrins. The Royal Society o

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