JOURNAL OF PORPHYRINS AND PHTHALOCYANINES (JPP) 涵盖了卟啉、酞菁和相关大环化合物的化学、物理、生物学和技术方面的研究。研究论文、评论文章和简短的交流涉及这些化合物的合成、光谱学、加工和应用。

The Journal of Porphyrins and Phthalocyanines (JPP) covers research on the chemistry, physics, biology, and technology of porphyrins, phthalocyanines, and related macrocyclic compounds. The journal publishes research papers, review articles, and short communications that address the synthesis, spectroscopy, processing, and applications of these compounds.

《Journal of Porphyrins and Phthalocyanines》涵盖了卟啉、酞菁及相关大环化合物在化学、物理、生物学和技术方面的研究。该期刊发表研究论文、评论文章和简短的交流，内容涉及这些化合物的合成、光谱学、加工及其应用。

Journal of Porphyrins and Phthalocyanines

A series of carbene ruthenium-porphyrins [ Ru ( por )(: CR 1 R 2 )] ( por = TPP ; R 1 = R 2 = p- C 6 H 4 Cl 2, p- C 6 H 4 Me 3, p- C 6 H 4 Ph 4; R 1 = Ph , R 2 = p- C 6 H 4 Ph 6; R 1 = Ph , R 2 = COPh 7; R 1 = p- C 6 H 4 Me , R 2 = CO (p- C 6 H 4 Me ) 8; R 1 = COMe, R 2 = COPh 9; por = TTP ; R 1 = R 2 = Ph 1', COPh 5') were synthesized and characterized. The starting material [ Ru ( por )( CO )] was treated with corresponding diazo compounds N 2 CR 1 R 2 in CH 2 Cl 2 or octane for the diaryl carbene complexes 1', 2-4 and 6, while it was subjected to photolysis in THF , followed by reflux with the diazo compounds for the acyl carbene complexes 5' and 7-9. The compounds were robust in octane under reflux and were able to catalyze cyclopropanation reactions with methyl diazoacetate (MDA) toward a wide variety of alkenes. Monocyclopropanation of 25 alkenes was demonstrated with catalyst 3 in octane under reflux. By reaction with more than equimolar amounts of MDA in the presence of catalyst 9, the first porphyrin-catalyzed biscyclopropanation was attained toward nonconjugated α, ω-dienes, viz. 1,5-hexadiene and 1,7-octadiene.

Satoko Wada

Masanobu Shimomura

Tomofumi Kikuchi

Hidetaka Yuge

T. Ken Miyamoto

Robust carbene ruthenium-porphyrin catalysts for cyclopropanation reaction of a wide variety of alkenes

适用于多种烯烃环丙烷化反应的鲁棒性卡宾钌卟啉催化剂

New mixed-substituent amino/carboxyphenylporphyrins for a dye-sensitized TiO 2 solar cell were prepared using several synthetic routes. The reaction of 4-carbomethoxy- and 4-acetamidobenzaldehydes with pyrrole in propionic acid under aerobic conditions afforded mixtures of mixed amide/ester substituted tetraphenylporphyrins which were separated using centrifugal chromatography then deprotected to give the target compounds. Condensation of p-nitrophenyldipyrromethane with 4-carbomethoxybenzaldehyde in CH 2 Cl 2 catalyzed by trifluoroacetic acid, followed by oxidation with dichlorodicyanoquinone gives trans-dicarbomethoxy/dinitrophenylporphyrin, which when treated with SnCl 2 and HCl affords the trans-diamino/dicarboxy derivative, trans- TA 2 C 2 PP . Commercially available tetrakis-5,10,15,20-(4-carboxyphenyl)porphyrin (TCPP) was converted to mixtures of mixed amino/carbomethoxyphenylporphyrins using hydroxylamine hydrochloride in polyphosphoric acid with methanol workup. Relative yields and product distributions from each route are discussed and the optoelectronic characteristics of the synthesized porphyrins were studied using UV-visible spectroscopy and cyclic voltammetry.

Michael G. Walter

Carl C. Wamser

Joseph Ruwitch

Yinping Zhao

Dale Braden

Matt Stevens

Al Denman

Rick Pi

Alexander Rudine

Peter J. Pessiki

Syntheses and optoelectronic properties of amino/carboxyphenylporphyrins for potential use in dye-sensitizedTiO2solar cells

氨基/羧基苯基卟啉的合成及其在染料敏化二氧化钛太阳能电池中的潜在应用的光电性能

A facile synthetic strategy was developed for the synthesis of meso -tetrakis(4-formyl-phenyl)porphyrin and meso -tetrakis(3-formylphenyl)porphyrin from commercially available starting materials. This method gives facile access to practical amounts of these synthons in high purity and good overall yield, without employing laborious chromatographic separations. The reduction of the respective carboxylic acid-functionalized porphyrins by LiAlH 4 afforded the tetra(benzylalcohol)porphyrin intermediates, subsequently utilized in a Parikh-Doering oxidation to selectively afford the desired tetraformylated products. The inherent ease of synthesis of these porphyrin building blocks provides a convenient pathway for the synthesis of various macromolecular and supramolecular architectures for applied chemical technologies.

Valentinos Mouarrawis

Simon Mathew

Eva J. Meeus

Bas de Bruin

Joost Reek

A chromatography-free synthesis of meso -tetrakis(4-formylphenyl)porphyrin and meso -tetrakis(3-formylphenyl)porphyrin: Versatile synthons in supramolecular and macromolecular chemistry

无色谱合成meso-四(4-甲醛苯基)卟啉和meso-四(3-甲醛苯基)卟啉：超分子和大分子化学中的多功能合成子

Mateusz Wozny

Monica Fresta

Jan Meffert

Annemieke Madder

Dorota Gryko

Vitamin B12 functionalized with hydroxy-pyrrol-2-one linkers

羟基吡咯-2-酮连接的维生素B12功能化

Xiao Yu

Chen Yuantao

Zhang Wei

Shao Liming

Nano titanium dioxide coating Haematococcus pluvialis enhances photoelectric carbon dioxide reduction performance

纳米二氧化钛涂层雨生红球藻增强光电二氧化碳还原性能

Shin Ogasawara

Yuki Egami

Koudai Yoshimura

Hitoshi Tamiaki

C132-Substitutions of methyl pheophorbides-a/a' by Michael addition reactions

通过迈克尔加成反应对甲基脱镁叶绿素-a/a'进行C132取代

Margaret W. Murage

Edith K. Amuhaya

Betty N. Mbatia

Edward K. Muge

Solomon Derese

Synergistic effect of porphyrin-induced photodynamic antimicrobial chemotherapy combined with gentamicin against clinically important gram-positive and gram-negative bacteria

卟啉诱导的光动力抗菌化疗与庆大霉素联合作用对临床重要革兰氏阳性和革兰氏阴性细菌的协同效应

Silve Dasgupta

Manne Naga Rajesh

Prakriti R. Bangal

Lingamallu Giribabu

Unraveling the relaxation dynamics of donor-π-acceptor porphyrins, achieving a promising 10.51% device efficiency in dye-sensitized solar cells

揭示供体-π-受体卟啉的弛豫动力学，实现染料敏化太阳能电池中10.51%的有前景的器件效率

Abbreviation	J. Porphyrins Phthalocyanines
Journal Impact	1.06
Quartiles(Global)	CHEMISTRY, MULTIDISCIPLINARY(Q4)

ISSN	1088-4246, 1099-1409
h-index	70

Publication Information	Publisher: World Scientific，Publishing cycle: Monthly，Journal Type: journal，Open Access Journals: No
Basic data	Year of publication: 1997，Proportion of original research papers: 98.36%，Self Citation Rate:22.20%， Gold OA Rate: 2.01%
Average review cycle	网友分享经验：平均1.0个月
Average recruitment ratio	网友分享经验：容易

Journal of Porphyrins and Phthalocyanines

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Robust carbene ruthenium-porphyrin catalysts for cyclopropanation reaction of a wide variety of alkenes

Syntheses and optoelectronic properties of amino/carboxyphenylporphyrins for potential use in dye-sensitizedTiO₂solar cells

A chromatography-free synthesis of meso -tetrakis(4-formylphenyl)porphyrin and meso -tetrakis(3-formylphenyl)porphyrin: Versatile synthons in supramolecular and macromolecular chemistry

Vitamin B₁₂ functionalized with hydroxy-pyrrol-2-one linkers

Nano titanium dioxide coating Haematococcus pluvialis enhances photoelectric carbon dioxide reduction performance

Vitamin B₁₂ functionalized with hydroxy-pyrrol-2-one linkers

Nano titanium dioxide coating Haematococcus pluvialis enhances photoelectric carbon dioxide reduction performance

C13²-Substitutions of methyl pheophorbides-a/a' by Michael addition reactions

Synergistic effect of porphyrin-induced photodynamic antimicrobial chemotherapy combined with gentamicin against clinically important gram-positive and gram-negative bacteria

Unraveling the relaxation dynamics of donor-π-acceptor porphyrins, achieving a promising 10.51% device efficiency in dye-sensitized solar cells