Core-Modified Rubyrins Containing Dithienylethene Moieties

Synthesis of a [26]Hexaphyrin Bis-PdIIComplex with a Characteristic Aromatic Circuit

(2013) Tomoki Yoneda et al.   CHEMISTRY-A EUROPEAN JOURNAL

SYNTHESIS AND CHARACTERIZATION OF TRIPHYRINS: A NEW FAMILY OF PORPHYRINOIDS

(2013) Hiroko Yamada et al.   HETEROCYCLES

Photoelectrocatalysis to Improve Cycloreversion Quantum Yields of Photochromic Dithienylethene Compounds

(2012) Sumin Lee et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Ruthenocenoporphyrinoids: Conformation Determines Macrocyclic π Conjugation Transmitted Across a d-Electron Metallocene

(2012) Irena Grocka et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

A 20π-Electron Heteroporphyrin Containing a Thienopyrrole Unit

(2012) Yi Chang et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Deprotonation-Induced Aromaticity Enhancement and New Conjugated Networks inmeso-Hexakis(pentafluorophenyl)[26]hexaphyrin

(2012) Won-Young Cha et al.   CHEMISTRY-A EUROPEAN JOURNAL

Syntheses and Fully Diastereospecific Photochromic Reactions of Thiophenophan-1-enes with Chiral Bridges

(2012) Hirotsugu Jin-nouchi et al.   CHEMISTRY-A EUROPEAN JOURNAL

Description of Aromaticity in Porphyrinoids

(2012) Judy I. Wu et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

How Should Aromaticity Be Described in Porphyrinoids?

(2011) Martin Bröring   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Figure Eights, Möbius Bands, and More: Conformation and Aromaticity of Porphyrinoids

(2011) Marcin Stępień et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Expanded Porphyrins: Intriguing Structures, Electronic Properties, and Reactivities

(2011) Shohei Saito et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Conformational and spectroscopic properties of π-extended, bipyrrole-fused rubyrin and sapphyrin derivatives

(2011) Se-Young Kee et al.   CHEMICAL COMMUNICATIONS

Expanded porphyrins and aromaticity

(2011) Atsuhiro Osuka et al.   CHEMICAL COMMUNICATIONS

Synthesis and Photochromic Properties of [2.2]Thiophenophan-8-ene-1,2-diol

(2011) Michinori Takeshita et al.   CHEMISTRY LETTERS

The Synthesis and Properties of Free-Base [14]Triphyrin(2.1.1) Compounds and the Formation of Subporphyrinoid Metal Complexes

(2011) Zhao Li Xue et al.   CHEMISTRY-A EUROPEAN JOURNAL

Solvent-Dependent Aromatic versus Antiaromatic Conformational Switching in meso-(Heptakis)pentafluorophenyl [32]Heptaphyrin

(2011) Min-Chul Yoon et al.   CHEMISTRY-A EUROPEAN JOURNAL

Highly Efficient Visible-Light Driven Photochromism: Developments towards a Solid-State Molecular Switch Operating through a Triplet-Sensitised Pathway

(2011) Simon K. Brayshaw et al.   CHEMISTRY-A EUROPEAN JOURNAL

Preparation and Characterization of Nonclassical Tetraazaporphyrin, Bis(4-methylpyridine)[1,3,5,7,9,11,13,15-octaphenyltetra(3,4-thieno)tetraazaporphyrinato]ruthenium(II)

(2011) Takeshi Kimura et al.   EUROPEAN JOURNAL OF INORGANIC CHEMISTRY

Diarylethene-Containing Cyclometalated Platinum(II) Complexes: Tunable Photochromism via Metal Coordination and Rational Ligand Design

(2011) Jacky Chi-Hung Chan et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

π Conjugation Transmitted across a d-Electron Metallocene in Ferrocenothiaporphyrin Macrocycles

(2010) Irena Simkowa et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Aromaticity and photophysical properties of various topology-controlled expanded porphyrins

(2010) Jae-Yoon Shin et al.   CHEMICAL SOCIETY REVIEWS

Switching the Cubic Nonlinear Optical Properties of an Electro-, Halo-, and Photochromic Ruthenium Alkynyl Complex Across Six States

(2009) Katy A. Green et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Amphiphilic Porphyrins for Second Harmonic Generation Imaging

(2009) James E. Reeve et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

A Facile One-Pot Synthesis ofmeso-Aryl-Substituted [14]Triphyrin(2.1.1)

(2008) Zhao-Li Xue et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

A Core-Modified Rubyrin withmeso-Aryl Substituents and Phenanthrene-Fused Pyrrole Rings: A Highly Conjugated Near-Infrared Dye and Hg2+ Probe

(2007) Di Wu et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION