Persistent microporosity of a non-planar porphyrinoid based on multiple supramolecular interactions for nanomechanical sensor applications

Mandeep K. Chahal, Subrata Maji, Anuradha Liyanage, Yoshitaka Matsushita, Pelin Tozman, Daniel T. Payne, Wipakorn Jevasuwan, Naoki Fukata, Paul A. Karr, Jan Labuta, Lok Kumar Shrestha, Shinsuke Ishihara, Katsuhiko Ariga, Francis D’Souza, Genki Yoshikawa, Yusuke Yamauchi and Jonathan P. Hill

Mater. Chem. Front., 2023, 7, 325
DOI: 10.1039/D2QM01039A

Nonplanar porphyrins: synthesis, properties, and unique functionalities

Tomoya Ishizuka, Nitika Grover, Christopher J. Kingsbury, Hiroaki Kotani, Mathias O. Senge and Takahiko Kojima

Chem. Soc. Rev., 2022, 51, 7560
DOI: 10.1039/D2CS00391K

Control of the spatial arrangements of supramolecular networks based on saddle-distorted porphyrins by intermolecular hydrogen bonding

Tomoya Ishizuka, Muniappan Sankar and Takahiko Kojima

Dalton Trans., 2013, 42, 16073
DOI: 10.1039/c3dt51467f

Structural and Interaction Properties of Porphyrin Layers — A Quantum Chemical Study

G. Praveena and A. Abiram

Commun. Theor. Phys., 2015, 63, 625
DOI: 10.1088/0253-6102/63/5/625

Color Change Effect in an Organic–Inorganic Hybrid Material Based on a Porphyrin Diacid

Bettina Wagner, Natalie Dehnhardt, Martin Schmid, Benedikt P. Klein, Lukas Ruppenthal, Philipp Müller, Malte Zugermeier, J. Michael Gottfried, Sina Lippert, Marc-Uwe Halbich, Arash Rahimi-Iman and Johanna Heine

J. Phys. Chem. C, 2016, 120, 28363
DOI: 10.1021/acs.jpcc.6b11188

Molekulares Engineering freier Porphyrinbasen als Liganden – das N‐H⋅⋅⋅X‐Bindungsmotiv in Tetrapyrrolen

Marc Kielmann and Mathias O. Senge

Angewandte Chemie, 2019, 131, 424
DOI: 10.1002/ange.201806281

Self‐Assembly of Coronene Bisimides: Mechanistic Insight and Chiral Amplification

Chidambar Kulkarni, Rajesh Munirathinam and Subi J. George

Chemistry A European J, 2013, 19, 11270
DOI: 10.1002/chem.201301251

Planar and Nonplanar Free‐Base Tetraarylporphyrins: β‐Pyrrole Substituents and Geometric Effects on Electrochemistry, Spectroelectrochemistry, and Protonation/Deprotonation Reactions in Nonaqueous Media

Yuanyuan Fang, P. Bhyrappa, Zhongping Ou and Karl M. Kadish

Chemistry A European J, 2014, 20, 524
DOI: 10.1002/chem.201303141

Molecular Engineering of Free‐Base Porphyrins as Ligands—The N−H⋅⋅⋅X Binding Motif in Tetrapyrroles

Marc Kielmann and Mathias O. Senge

Angew Chem Int Ed, 2019, 58, 418
DOI: 10.1002/anie.201806281

Efficient Near‐Infrared‐Light‐Driven H2 Production with Salts of a Diprotonated Saddle‐Distorted Porphyrin as Photosensitizers

Hiroaki Kotani, Takuya Miyazaki, Takumi Ehara, Yasutaka Kitahama, Hiroyuki Matsuzaki, Kiyoshi Miyata, Ken Onda, Hayato Sakai, Taku Hasobe, Yoshihito Shiota, Kazunari Yoshizawa and Takahiko Kojima

ChemPhotoChem, 2025
DOI: 10.1002/cptc.202500009

Functional supramolecular systems: design and applications

Igor S. Antipin, Mikhail V. Alfimov, Vladimir V. Arslanov, Vladimir A. Burilov, Sergey Z. Vatsadze, Yan Z. Voloshin, Konstantin P. Volcho, Valery V. Gorbatchuk, Yulia G. Gorbunova, Sergey P. Gromov, Semyon V. Dudkin, Sergei Yu. Zaitsev, Lucia Ya. Zakharova, Marat A. Ziganshin, Anna V. Zolotukhina, Maria A. Kalinina, Eduard A. Karakhanov, Ruslan R. Kashapov, Oskar I. Koifman, Alexander I. Konovalov, Vladimir S. Korenev, Anton L. Maksimov, Nugzar Zh. Mamardashvili, Galina M. Mamardashvili, Alexander G. Martynov, Asiya R. Mustafina, Ramil I. Nugmanov, Alexander S. Ovsyannikov, Pavel L. Padnya, Andrei S. Potapov, Sofiya L. Selektor, Maxim N. Sokolov, Svetlana E. Solovieva, Ivan I. Stoikov, Pavel A. Stuzhin, Evgenii V. Suslov, Evgeny N. Ushakov, Vladimir P. Fedin, Svetlana V. Fedorenko, Olga A. Fedorova, Yury V. Fedorov, Sergei N. Chvalun, Aslan Yu. Tsivadze, Sergei N. Shtykov, Dmitriy N. Shurpik, Maxim A. Shcherbina and Luidmila S. Yakimova

Russ. Chem. Rev., 2021, 90, 895
DOI: 10.1070/RCR5011