Carbazole-containing porphyrinoid and its oligomers

Tongjing Wu, Taeyeon Kim, Bangshao Yin, Kaisheng Wang, Ling Xu, Mingbo Zhou, Dongho Kim and Jianxin Song

Chem. Commun., 2019, 55, 11454
DOI: 10.1039/C9CC06114B

Magnetic exchange coupling of a synthetic Co(ii)-complex to a ferromagnetic Ni substrate

Christian Wäckerlin, Pablo Maldonado, Lena Arnold, Aneliia Shchyrba, Jan Girovsky, Jan Nowakowski, Md. Ehesan Ali, Tatjana Hählen, Milos Baljozovic, Dorota Siewert, Armin Kleibert, Klaus Müllen, Peter M. Oppeneer, Thomas A. Jung and Nirmalya Ballav

Chem. Commun., 2013, 49, 10736
DOI: 10.1039/c3cc45401k

Tuneable reversible redox of cobalt(iii) carbazole complexes

Michael S. Bennington, Humphrey L. C. Feltham, Zoë J. Buxton, Nicholas G. White and Sally Brooker

Dalton Trans., 2017, 46, 4696
DOI: 10.1039/C7DT00295E

A route to a cyclobutane-linked double-looped system via a helical macrocycle

Jan Klajn, Wojciech Stawski, Piotr J. Chmielewski, Joanna Cybińska and Miłosz Pawlicki

Chem. Commun., 2019, 55, 4558
DOI: 10.1039/C9CC01201J

Synthesis and electronic properties of carbazole-based core-modified diporphyrins showing near infrared absorption

Chihiro Maeda, Takuma Shirakawa and Tadashi Ema

Chem. Commun., 2020, 56, 15048
DOI: 10.1039/D0CC06289H

Quantifying near-symmetric molecular distortion using symmetry-coordinate structural decomposition

Christopher J. Kingsbury and Mathias O. Senge

Chem. Sci., 2024, 15, 13638
DOI: 10.1039/D4SC01670J

Synthesis of carbazole-based hetero-core-modified porphyrins

Chihiro Maeda, Motoki Masuda and Naoki Yoshioka

Org. Biomol. Chem., 2014, 12, 2656
DOI: 10.1039/C3OB42564A

Effects of cyano, ethynyl and ethylenedioxy groups on the photophysical properties of carbazole-based porphyrins

Chihiro Maeda, Kosuke Kurihara, Motoki Masuda and Naoki Yoshioka

Org. Biomol. Chem., 2015, 13, 11286
DOI: 10.1039/C5OB01824B

Bright luminescent lithium and magnesium carbene complexes

Piermaria Pinter, Christoph M. Schüßlbauer, Fabian A. Watt, Nicole Dickmann, Regine Herbst-Irmer, Bernd Morgenstern, Annette Grünwald, Tobias Ullrich, Michael Zimmer, Stephan Hohloch, Dirk M. Guldi and Dominik Munz

Chem. Sci., 2021, 12, 7401
DOI: 10.1039/D1SC00846C

Conformationally restricted and three-dimensionally extended carbazole-incorporating expanded porphyrinoids

Feilong Li, Kaisheng Wang, Yutao Rao, Ling Xu, Atsuhiro Osuka and Jianxin Song

Org. Chem. Front., 2022, 9, 4798
DOI: 10.1039/D2QO00834C

A carbazole-containing porphyrinoid: synthesis and oxidation to the porphyrin-state

Lena Arnold, Martin Baumgarten and Klaus Müllen

Chem. Commun., 2012, 48, 9640
DOI: 10.1039/c2cc35550g

π-Extended isomeric and expanded porphyrins

Vladimir V. Roznyatovskiy, Chang-Hee Lee and Jonathan L. Sessler

Chem. Soc. Rev., 2013, 42, 1921
DOI: 10.1039/C2CS35418G

New ruthenium(ii) catalysts enable the synthesis of 2-amino-4H-chromenes using primary alcohols via acceptorless dehydrogenative coupling

Veerappan Tamilthendral, Rengan Ramesh and Jan Grzegorz Malecki

New J. Chem., 2022, 46, 21568
DOI: 10.1039/D2NJ03268F

Synthesis and oxidation of cyclic tetraindole

Shoichi Nakamura, Satoru Hiroto and Hiroshi Shinokubo

Chem. Sci., 2012, 3, 524
DOI: 10.1039/C1SC00665G

Peripherally ethynylated carbazole-based core-modified porphyrins

Chihiro Maeda and Naoki Yoshioka

Org. Biomol. Chem., 2012, 10, 5182
DOI: 10.1039/c2ob25645b

Carbazole-based N4-donor Schiff base macrocycles: obtained metal free and as Cu(ii) and Ni(ii) complexes

Stuart J. Malthus, Rajni K. Wilson, A. Vikas Aggarwal, Scott A. Cameron, David S. Larsen and Sally Brooker

Dalton Trans., 2017, 46, 3141
DOI: 10.1039/C6DT04598G

Advent and features of pyriporphyrinoids: an overview of a pyridine-based porphyrin analogue

Mainak Das and A. Srinivasan

Chem. Commun., 2023, 59, 11780
DOI: 10.1039/D3CC03139J

Synthesis and electronic properties of π-expanded carbazole-based porphyrins

Chihiro Maeda, Yumi Tanaka, Takuma Shirakawa and Tadashi Ema

Chem. Commun., 2019, 55, 10162
DOI: 10.1039/C9CC05079E

Pyrrole-contained fused-ring compounds

Zhi-Ao Li, Li-Jun Peng, Xin-Yue Wang and Han-Yuan Gong

J. Porphyrins Phthalocyanines, 2023, 27, 980
DOI: 10.1142/S1088424623300094

Synthesis of Carbazole‐Containing Porphyrinoids by a Multiple Annulation Strategy: A Core‐Modified and π‐Expanded Porphyrin

Chihiro Maeda, Tomoki Yoneda, Naoki Aratani, Min‐Chul Yoon, Jong Min Lim, Dongho Kim, Naoki Yoshioka and Atsuhiro Osuka

Angew Chem Int Ed, 2011, 50, 5691
DOI: 10.1002/anie.201101864

Intramolecular Electronic Coupling in the Thiophene-Bridged Carbazole-Based Diporphyrin

Chihiro Maeda, Mototsugu Takata, Asami Honsho and Tadashi Ema

Org. Lett., 2016, 18, 6070
DOI: 10.1021/acs.orglett.6b03054

LNL-Carbazole Pincer Ligand: More than the Sum of Its Parts

George Kleinhans, Aino J. Karhu, Hugo Boddaert, Sadia Tanweer, David Wunderlin and Daniela I. Bezuidenhout

Chem. Rev., 2023, 123, 8781
DOI: 10.1021/acs.chemrev.3c00202

Bipyricorrole: A Corrole Homologue with a Monoanionic Core as a Fluorescence ZnII Sensor

B. Adinarayana, Ajesh P. Thomas, Prerna Yadav, Arun Kumar and A. Srinivasan

Angew Chem Int Ed, 2016, 55, 969
DOI: 10.1002/anie.201508829

Fluctuating exciton localization in giant π-conjugated spoked-wheel macrocycles

A. Vikas Aggarwal, Alexander Thiessen, Alissa Idelson, Daniel Kalle, Dominik Würsch, Thomas Stangl, Florian Steiner, Stefan-S. Jester, Jan Vogelsang, Sigurd Höger and John M. Lupton

Nature Chem, 2013, 5, 964
DOI: 10.1038/nchem.1758

Macrocyclic Amine‐Linked Oligocarbazole Hollow Microspheres: Facile Synthesis and Efficient Lead Sorbents

Yaozu Liao, Sisi Cai, Shaojun Huang, Xia Wang and Charl F. J. Faul

Macromol. Rapid Commun., 2014, 35, 1833
DOI: 10.1002/marc.201400415

Organische Chemie 2011

Nachr Chem, 2012, 60, 265
DOI: 10.1002/nadc.201290119

First row transition metal complexes of di-o-substituted-diarylamine-based ligands (including carbazoles, acridines and dibenzoazepines)

Stuart J. Malthus, Scott A. Cameron and Sally Brooker

Coordination Chemistry Reviews, 2016, 316, 125
DOI: 10.1016/j.ccr.2016.02.006

Porphyrin Analogues That Consist of Indole, Benzofuran, and Benzothiophene Subunits

Shoichi Nakamura, Takeshi Kondo, Satoru Hiroto and Hiroshi Shinokubo

Asian J Org Chem, 2013, 2, 312
DOI: 10.1002/ajoc.201300033

Coordination chemistry and application of mono- and oligopyridine-based macrocycles

Ashanul Haque, Rashid Ilmi, Idris Juma Al-Busaidi and Muhammad S. Khan

Coordination Chemistry Reviews, 2017, 350, 320
DOI: 10.1016/j.ccr.2017.07.008

Stable Inner 2H Tautomer of N-Confused-like Porphyrin Embedded with a Carbazole Subunit: Synthesis, Metal Coordination, and Magnetic and Anion Sensing Studies

Arumugam Kalaiselvan, Athira Naniyil, Ruth Mariam Ipe, Sai Vamsi Krishna Isukapalli, Sivaranjana Reddy Vennapusa, Alex P. Andrews and Sabapathi Gokulnath

J. Org. Chem., 2023, 88, 14377
DOI: 10.1021/acs.joc.3c01255

Shape‐Assisted Self‐Assembly of Hexa‐Substituted Carpyridines into 1D Supramolecular Polymers

Lucía Gallego, Joseph F. Woods, Rachele Butti, Piotr Szwedziak, Andreas Vargas Jentzsch and Michel Rickhaus

Angewandte Chemie, 2024, 136
DOI: 10.1002/ange.202318879

Fused π-extended discotic triangular porphyrinoids

Lena Arnold, Sreenivasa Reddy Puniredd, Christian von Malotki, Wojciech Pisula, Nobuyoshi Koshino, Hideyuki Higashimura, Martin Baumgarten, Manfred Wagner and Klaus Müllen

J. Porphyrins Phthalocyanines, 2012, 16, 564
DOI: 10.1142/S1088424612500629

Designing π-conjugated polymers for organic electronics

Xin Guo, Martin Baumgarten and Klaus Müllen

Progress in Polymer Science, 2013, 38, 1832
DOI: 10.1016/j.progpolymsci.2013.09.005

Modifying the porphyrin core — a chemist's jigsaw

Lena Arnold and Klaus Müllen

J. Porphyrins Phthalocyanines, 2011, 15, 757
DOI: 10.1142/S1088424611003720

Synthesis of putative clausenal from carbazole using sequential C–H borylations

Jessica Liyu and Jonathan Sperry

Tetrahedron Letters, 2017, 58, 1699
DOI: 10.1016/j.tetlet.2017.03.051

Synthesis and Functionalization of Porphyrins through Organometallic Methodologies

Satoru Hiroto, Yoshihiro Miyake and Hiroshi Shinokubo

Chem. Rev., 2017, 117, 2910
DOI: 10.1021/acs.chemrev.6b00427

Shallow Rate-Redox Potential Scaling in Aqueous Molecular Oxygen Reduction Electrocatalysis Across a Family of Iron Macrocycles

Travis Marshall-Roth, Liang Liu, Vennela Mannava, Deiaa M. Harraz, Brian J. Cook, R. Morris Bullock and Yogesh Surendranath

ACS Catal., 2024, 14, 18590
DOI: 10.1021/acscatal.4c06561

Efficient Synthesis oftert-Butyl (6-Formylpyridin-2-yl)carbamic Acid

Helena Majgier-Baranowska, Bing Li and Norton P. Peet

Synthetic Communications, 2013, 43, 1173
DOI: 10.1080/00397911.2011.625291

Low‐Valent Zirconocene‐Mediated Synthesis of Porphyrin(2.1.2.1)s and Its Extension to Synthesis of a Porphyrin(2.1.2.1) Nanobarrel

Yidan Wu, Tingting Zhao, Jian Rong, Yutao Rao, Mingbo Zhou, Bangshao Yin, Xinlong Ni, Atsuhiro Osuka, Ling Xu and Jianxin Song

Angew Chem Int Ed, 2022, 61
DOI: 10.1002/anie.202201327

Reductive Dimerization of Macrocycles Activated by BBr3

Monika Kijewska, Miłosz Siczek and Miłosz Pawlicki

Org. Lett., 2021, 23, 3652
DOI: 10.1021/acs.orglett.1c01047

Metal ion effect on the supramolecular structures of metalloporphyrins on single-walled carbon nanotube surface

Ahmed I. A. Abd El-Mageed and Takuji Ogawa

Applied Surface Science, 2018, 462, 904
DOI: 10.1016/j.apsusc.2018.08.177

Highly Conductive Single-Molecule Wires with Controlled Orientation by Coordination of Metalloporphyrins

Albert C. Aragonès, Nadim Darwish, Wojciech J. Saletra, Lluïsa Pérez-García, Fausto Sanz, Josep Puigmartí-Luis, David B. Amabilino and Ismael Díez-Pérez

Nano Lett., 2014, 14, 4751
DOI: 10.1021/nl501884g

Color‐Tunable Solid‐State Fluorescence Emission from Carbazole‐Based BODIPYs

Chihiro Maeda, Takumi Todaka, Tomomi Ueda and Tadashi Ema

Chemistry A European J, 2016, 22, 7508
DOI: 10.1002/chem.201505150

Carbazole-Based Porphyrins: Synthesis, Structure–Photophysical Property Correlations, and Mercury Ion Sensing

Arumugam Kalaiselvan, Isukapalli Sai Vamsi Krishna, Anjana Prasad Nambiar, Aathira Edwin, Vennapusa Sivaranjana Reddy and Sabapathi Gokulnath

Org. Lett., 2020, 22, 4494
DOI: 10.1021/acs.orglett.0c01500

Synthesis of Carbazole‐Containing Porphyrinoids by a Multiple Annulation Strategy: A Core‐Modified and π‐Expanded Porphyrin

Chihiro Maeda, Tomoki Yoneda, Naoki Aratani, Min‐Chul Yoon, Jong Min Lim, Dongho Kim, Naoki Yoshioka and Atsuhiro Osuka

Angewandte Chemie, 2011, 123, 5809
DOI: 10.1002/ange.201101864

Carbenaporphyrine: eine Lücke in der Chemie N‐heterocyclischer Carbene schließt sich

Theo Maulbetsch and Doris Kunz

Angewandte Chemie, 2021, 133, 2035
DOI: 10.1002/ange.202013434

Conjugated Macrocycles: Concepts and Applications

Masahiko Iyoda, Jun Yamakawa and M. Jalilur Rahman

Angew Chem Int Ed, 2011, 50, 10522
DOI: 10.1002/anie.201006198

Synthetic aspects of carbazole containing porphyrins and porphyrinoids

Sudipta Das and Iti Gupta

J. Porphyrins Phthalocyanines, 2019, 23, 367
DOI: 10.1142/S1088424619300052

Konjugierte Makrocyclen: Konzepte und Anwendungen

Masahiko Iyoda, Jun Yamakawa and M. Jalilur Rahman

Angewandte Chemie, 2011, 123, 10708
DOI: 10.1002/ange.201006198

Low‐Valent Zirconocene‐Mediated Synthesis of Porphyrin(2.1.2.1)s and Its Extension to Synthesis of a Porphyrin(2.1.2.1) Nanobarrel

Yidan Wu, Tingting Zhao, Jian Rong, Yutao Rao, Mingbo Zhou, Bangshao Yin, Xinlong Ni, Atsuhiro Osuka, Ling Xu and Jianxin Song

Angewandte Chemie, 2022, 134
DOI: 10.1002/ange.202201327

Synthesis and Characterization of Novel Fused Porphyrinoids Based on Cyclic Carbazole[2]indolones

Chihiro Maeda and Naoki Yoshioka

Org. Lett., 2012, 14, 2122
DOI: 10.1021/ol300585v

Carbenaporphyrins: No Longer Missing Ligands in N‐Heterocyclic Carbene Chemistry

Theo Maulbetsch and Doris Kunz

Angew Chem Int Ed, 2021, 60, 2007
DOI: 10.1002/anie.202013434

Calix[2]bispyrrolylarenes: New Expanded Calix[4]pyrroles for Fluorometric Sensing of Anions via Extended π-Conjugation

Brijesh Chandra, Sanjeev P. Mahanta, Narendra N. Pati, Sambath Baskaran, Ravi K. Kanaparthi, Chinnappan Sivasankar and Pradeepta K. Panda

Org. Lett., 2013, 15, 306
DOI: 10.1021/ol3032158

Multifunctional Tricarbazolo Triazolophane Macrocycles: One‐Pot Preparation, Anion Binding, and Hierarchical Self‐Organization of Multilayers

Semin Lee, Brandon E. Hirsch, Yun Liu, James R. Dobscha, David W. Burke, Steven L. Tait and Amar H. Flood

Chemistry A European J, 2016, 22, 560
DOI: 10.1002/chem.201503161

Shape‐Assisted Self‐Assembly of Hexa‐Substituted Carpyridines into 1D Supramolecular Polymers

Lucía Gallego, Joseph F. Woods, Rachele Butti, Piotr Szwedziak, Andreas Vargas Jentzsch and Michel Rickhaus

Angew Chem Int Ed, 2024, 63
DOI: 10.1002/anie.202318879

Structural and Electronic Tuning of Luminescent ZnII Complexes Based on an o-Terphenyl Ligand Motif

Darius A. Shariaty, Peter I. Djurovich and Mark E. Thompson

J. Am. Chem. Soc., 2025, 147, 29065
DOI: 10.1021/jacs.5c07162

3,6-Carbazoylene Octaphyrin (1.0.0.0.1.0.0.0) and Its Bis-BF2 Complex

Hao Chen, Xusheng Shi, Yipeng Lun, Yan Xu, Tian Lu, Zhiming Duan, Min Shao, Jonathan L. Sessler, Huakang Yu and Chuanhu Lei

J. Am. Chem. Soc., 2022, 144, 8194
DOI: 10.1021/jacs.2c01240

Preorganized Anion Traps for Exploiting Anion–π Interactions: An Experimental and Computational Study

Anne Bretschneider, Diego M. Andrada, Sebastian Dechert, Steffen Meyer, Ricardo A. Mata and Franc Meyer

Chemistry A European J, 2013, 19, 16988
DOI: 10.1002/chem.201302598

2-(Naphthalen-1-yl)thiophene as a New Motif for Porphyrinoids: Meso-Fused Carbaporphyrin

Jung-Ho Hong, Adil S. Aslam, Masatoshi Ishida, Shigeki Mori, Hiroyuki Furuta and Dong-Gyu Cho

J. Am. Chem. Soc., 2016, 138, 4992
DOI: 10.1021/jacs.6b01063

Heterocyclic Nanographenes and Other Polycyclic Heteroaromatic Compounds: Synthetic Routes, Properties, and Applications

Marcin Stępień, Elżbieta Gońka, Marika Żyła and Natasza Sprutta

Chem. Rev., 2017, 117, 3479
DOI: 10.1021/acs.chemrev.6b00076

Cyclo[m]pyridine[n]pyrroles: Hybrid Macrocycles That Display Expanded π-Conjugation upon Protonation

Zhan Zhang, Jong Min Lim, Masatoshi Ishida, Vladimir V. Roznyatovskiy, Vincent M. Lynch, Han-Yuan Gong, Xiaoping Yang, Dongho Kim and Jonathan L. Sessler

J. Am. Chem. Soc., 2012, 134, 4076
DOI: 10.1021/ja211985k

Palladium Complexes of Carbazole‐Based Chalcogenaisophlorins: Synthesis, Structure, and Solid‐State NIR Absorption Spectra

Chihiro Maeda, Kazuto Takaishi and Tadashi Ema

ChemPlusChem, 2017, 82, 1368
DOI: 10.1002/cplu.201700430

Effective π-Extension of Carbazole-Based Thiaporphyrins by Peripheral Phenylethynyl Substituents

Chihiro Maeda, Mikako Masuda and Naoki Yoshioka

Org. Lett., 2013, 15, 3566
DOI: 10.1021/ol401403n

Non‐Planar [n]Cyclo‐1,8‐carbazolylenes (n=3,4,6) and [3]Cyclo‐1,8‐carbazolylenyl B, P, PO, SiPh Complexes

Koji Yamamoto, Palash Pandit and Shuhei Higashibayashi

Chemistry A European J, 2017, 23, 14011
DOI: 10.1002/chem.201702853

Synthesis and Characterization of Carbazole‐Based Expanded Thiaporphyrins

Motoki Masuda and Chihiro Maeda

Chemistry A European J, 2013, 19, 2971
DOI: 10.1002/chem.201202573

Shape-assisted self-assembly

Joseph F. Woods, Lucía Gallego, Pauline Pfister, Mounir Maaloum, Andreas Vargas Jentzsch and Michel Rickhaus

Nat Commun, 2022, 13
DOI: 10.1038/s41467-022-31482-2

Bipyricorrole: A Corrole Homologue with a Monoanionic Core as a Fluorescence ZnII Sensor

B. Adinarayana, Ajesh P. Thomas, Prerna Yadav, Arun Kumar and A. Srinivasan

Angewandte Chemie, 2016, 128, 981
DOI: 10.1002/ange.201508829

A Supramolecular Nanosheet Assembled from Carpyridines and Water

Joseph F. Woods, Kai Zhang, Joëlle Peterschmitt, Olivier Blacque, Céline Besnard, Gustavo Santiso-Quinones, Laura Samperisi, Andreas Vargas Jentzsch and Michel Rickhaus

J. Am. Chem. Soc., 2025, 147, 18380
DOI: 10.1021/jacs.4c17024

Synthesis of Carbazole-Based Selenaporphyrin via Annulation

Motoki Masuda, Chihiro Maeda and Naoki Yoshioka

Org. Lett., 2013, 15, 578
DOI: 10.1021/ol303392g