Sn(IV) meso-Tetraphenylporphine dichloride (contains 1-3% chlorin)

Product Number: 41359; CAS Number: 26334-85-0

$36.00$171.00

$36.00
$71.00
$105.00
$171.00

Sn(IV) meso-Tetraphenylporphine dichloride (contains 1-3% chlorin) CAS: 26334-85-0 MDL: MFCD00995672

Molecular weight: 802.34 g/mol

Molecular Formula: C44H28Cl2N4Sn

CAS Number: 26334-85-0

Storage: Store at room temperature, protect from light

Synonyms: Chlorure 5,10,15,20-tétraphénylporphine-21,22-diide d’étain(4+) (2:1:1), Tin(4+) chloride 5,10,15,20-tetraphenylporphine-21,22-diide (1:2:1), Zinn(4+)chlorid-5,10,15,20-tetraphenylporphin-21,22-diid (1:2:1), 26334-85-0, MESO-TETRAPHENYLPORPHYRIN-SN(IV)DICHLORIDE, Sn-Tpph, Tetraphenylporphyrin-Sn(4+),Tin, (5,10,15,20-tetraphenyl-21H,23H-porphinato(2-)-N21,N22,N23,N24)-, (SP-4-1)-

Field of Interest: Catalysis, Metal-Organic Frameworks, Photophysics

Background: Sn(IV) meso-Tetraphenylporphine dichloride (contains 1-3% chlorin) is a synthetic porphyrin specialty chemical manufactured by Frontier Specialty Chemicals.

References: 

1.) Zhong, et al. Interfacial Self-Assembly Driven Formation of Hierarchically Structured Nanocrystals with Photocatalytic Activity. ACS Nano 2014, 8, 1, 827–833. https://doi.org/10.1021/nn405492d

2.) Baral, et al. Tin(IV)-Porphyrin Tetracarbonyl Cobaltate: An Efficient Catalyst for the Carbonylation of Epoxides. Catalysts 2019, 9(4), 311; https://doi.org/10.3390/catal9040311

3.) Johnson, et al. Porphyrin-Metalation-Mediated Tuning of Photoredox Catalytic Properties in Metal-Organic Frameworks. ACS Catalysis, 2015, vol. 5, # 9, p. 5283 – 5291. https://doi.org/10.1021/acscatal.5b00941

4.) Moghadam, et al. Rapid and efficient acetylation of alcohols and phenols with acetic anhydride catalyzed by electron-deficient tin(IV) porphyrin. Journal of Molecular Catalysis A: Chemical, 2004, vol. 219, # 1, p. 73 – 78. https://doi.org/10.1016/j.molcata.2007.05.012

5.) Slagt, et al. Supramolecular bidentate phosphorus ligands based on bis-zinc(ii) and bis-tin(iv) porphyrin building blocks. Dalton Transactions, 2007, # 22, p. 2302 – 2310. https://doi.org/10.1039/B702462M

6.) Arnold, et al. Tin porphyrins. 6. Tin-119 chemical shifts and line widths of tin(IV) complexes of tetraphenyl-, tetra-p-tolyl-, and octaethylporphyrin. Inorganic Chemistry, 1994, vol. 33, # 7, p. 1486 – 1490. https://doi.org/10.1021/ic00085a044

7.) Maiti, et al. Photophysics of soret-excited tetrapyrroles in solution. IV. Radiationless decay and triplet-triplet annihilation investigated using tetraphenylporphinato Sn(IV)Journal of Physical Chemistry A, 2009, vol. 113, # 42, p. 11318 – 11326. https://doi.org/10.1021/jp906966h

8.) Olsson, et al. Design of oxophilic metalloporphyrins: An experimental and DFT study of methanol binding. Dalton Transactions, 2018, vol. 47, # 33, p. 11572 – 11585. https://doi.org/10.1039/C8DT02432D

Categories

Functional Groups

Metal

Porphyrin Family

A4 Porphyrins, Metallo Porphyrins, Tetra-Phenyl Porphine Derivatives

Porphyrin Substitution

Meso-Substituted Porphyrins, Phenyl Substituted Porphyrins

You may also like…

Shopping Cart
Scroll to Top