4.8 Article

Piperazine Bridged Thianorrole Dimer

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Chemistry, Multidisciplinary

Antiaromatic Sapphyrin Isomer: Transformation into Contracted Porphyrinoids with Variable Aromaticity

Qizhao Li et al.

Summary: In this study, we report the synthesis of a 20 pi antiaromatic sapphyrin isomer, which exhibits a reactivity for further oxidation due to its distinct antiaromatic electronic structure. The resulting compound possesses a unique spiro-carbon-containing [5.6.5.6]-tetracyclic structure and can be easily transformed to novel porphyrinoids with variable aromaticity. This research highlights the synthesis of porphyrinoid compounds with different aromatic properties.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2023)

Article Chemistry, Organic

Doubly Fused Unsymmetrical Calixdicarbahexaphyrins

Shubham Tiwari et al.

Summary: A series of novel doubly fused unsymmetrical calixdicarbahexaphyrins were synthesized through acid-catalyzed condensation. The macrocycles exhibited unsymmetrical structure with unusual fusions and disrupted π-electron delocalization. Experimental and theoretical studies confirmed their characteristics and properties.

JOURNAL OF ORGANIC CHEMISTRY (2022)

Article Chemistry, Organic

Synthesis of meso-Triaryl 22-Oxanorroles

Poornenth Pushpanandan et al.

Summary: Aromatic meso-triaryl-22-oxanorroles containing a pyrrole N-pyrrole alpha-C direct bond were successfully synthesized using a straightforward route. The synthesis method has a yield of 4-7% and provides an important basis for further research.

ORGANIC LETTERS (2022)

Article Chemistry, Multidisciplinary

Synthesis, Structure and Studies of Meso-Triaryl 22-Oxabenzonorroles

Vratta Grover et al.

Summary: In this study, a series of meso-triaryl 22-oxabenzonorroles were successfully synthesized and their structures and properties were investigated. The results demonstrated that these compounds exhibited strong absorption and electron-rich nature, which were supported by theoretical simulations.

CHEMISTRY-AN ASIAN JOURNAL (2022)

Review Chemistry, Multidisciplinary

Neo-Porphyrinoids: New Members of the Porphyrinoid Family

Poornenth Pushpanandan et al.

Summary: Porphyrins can have multiple possible isomers, with neoporphyrinoids being a newly discovered structural analogue. Different types of neoporphyrinoids have been synthesized using rational methodologies, and their properties have been studied in terms of spectral, structural, aromatic, and coordination aspects. There is significant potential for developing new synthetic routes to produce stable neoporphyrinoids for further exploration of their properties and potential applications.

TOPICS IN CURRENT CHEMISTRY (2021)

Review Chemistry, Multidisciplinary

Classic highlights in porphyrin and porphyrinoid total synthesis and biosynthesis

Mathias O. Senge et al.

Summary: Porphyrins play crucial roles in nature and modern applications, with their photochemical properties determining the biochemical functions of plants. Through complexation with metals, they can be utilized in various contemporary applications such as solar energy generation.

CHEMICAL SOCIETY REVIEWS (2021)

Article Chemistry, Multidisciplinary

Copper 1,19-Diaza-21,24-dicarbacorrole: A Corrole Analogue with an N-N Linkage Stabilizes a Ground-State Singlet Organocopper Species

Biju Basumatary et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2020)

Review Chemistry, Inorganic & Nuclear

Synthesis, characterization, and reactivities of high valent metal-corrole (M = Cr, Mn, and Fe) complexes

Sruti Mondal et al.

COORDINATION CHEMISTRY REVIEWS (2019)

Article Chemistry, Multidisciplinary

Ground-State Copper(III) Stabilized by N-Confused/N-Linked Corroles: Synthesis, Characterization, and Redox Reactivity

Yogesh Kumar Maurya et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2018)

Article Chemistry, Multidisciplinary

A Parallel-Displaced Directly Linked 21-Carba-23-Thiaporphyrin Dimer Incorporating a Dihydrofulvalene Motif

Anna Berlicka et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2016)

Article Chemistry, Multidisciplinary

Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers

Santosh C. Gadekar et al.

CHEMICAL COMMUNICATIONS (2016)

Article Chemistry, Multidisciplinary

Metal-Assisted Cyclomerization of N-Confused Dipyrrins into Expanded Norroles

Santosh C. Gadekar et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2013)

Article Chemistry, Multidisciplinary

Synthesis of a neo-confused porphyrin and an unusual dihydroporphyrin derivative

Ruoshi Li et al.

CHEMICAL COMMUNICATIONS (2013)

Article Chemistry, Multidisciplinary

Macrocycle Contraction and Expansion of a Dihydrosapphyrin Isomer

Yongshu Xie et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2013)

Article Chemistry, Multidisciplinary

Unique Interaction between Directly Linked Laminated p Planes in the Benzonorrole Dimer

Motoki Toganoh et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2012)

Article Chemistry, Multidisciplinary

Confusion and Neo-Confusion: Corrole Isomers with an NNNC Core

Keitaro Fujino et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2011)

Review Chemistry, Inorganic & Nuclear

Coordination chemistry of corroles with focus on main group elements

Iris Aviv-Hare et al.

COORDINATION CHEMISTRY REVIEWS (2011)

Article Chemistry, Inorganic & Nuclear

Protonated N-Confused Porphyrin Dimer: Formation, Structure, and Guest Binding

Piotr J. Chmielewski et al.

INORGANIC CHEMISTRY (2011)

Article Chemistry, Organic

C-Fused Norrole: A Fused Corrole Isomer Bearing a N,C-Linked Bipyrrole Unit

Motold Toganoh et al.

JOURNAL OF ORGANIC CHEMISTRY (2011)

Review Chemistry, Multidisciplinary

Aura of Corroles

Iris Aviv-Harel et al.

CHEMISTRY-A EUROPEAN JOURNAL (2009)

Article Chemistry, Multidisciplinary

Synthesis and characterization of a directly linked N-confused porphyrin dimer

PJ Chmielewski

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2004)

Article Chemistry, Organic

A facile, highly efficient synthesis of fully N-confused calix[5]pyrrole

QQ Chen et al.

SYNTHETIC COMMUNICATIONS (2002)