Topology Switching in [32]Heptaphyrins Controlled by Solvent, Protonation, andmeso Substituents

Viability of Möbius Topologies in [26]- and [28]Hexaphyrins

(2012) Mercedes Alonso et al.   CHEMISTRY-A EUROPEAN JOURNAL

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

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

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

Density-functional approaches to noncovalent interactions: A comparison of dispersion corrections (DFT-D), exchange-hole dipole moment (XDM) theory, and specialized functionals

(2011) Lori A. Burns et al.   JOURNAL OF CHEMICAL PHYSICS

NCIPLOT: A Program for Plotting Noncovalent Interaction Regions

(2011) Julia Contreras-García et al.   Journal of Chemical Theory and Computation

Metal Complexes of Chiral Möbius Aromatic [28]Hexaphyrin(1.1.1.1.1.1): Enantiomeric Separation, Absolute Stereochemistry, and Asymmetric Synthesis

(2010) Takayuki Tanaka 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

meso-Trifluoromethyl-substituted Subporphyrin from Ring-splitting Reaction ofmeso-Trifluoromethyl-substituted [32]Heptaphyrin(1.1.1.1.1.1.1)

(2010) Ryu Sakamoto et al.   CHEMISTRY LETTERS

A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu

(2010) Stefan Grimme et al.   JOURNAL OF CHEMICAL PHYSICS

Theoretical Study on Conformation and Electronic State of Hückel-Aromatic Multiply N-Confused [26]Hexaphyrins

(2010) Motoki Toganoh et al.   JOURNAL OF ORGANIC CHEMISTRY

Protonated [4n]π and [4n+2]π Octaphyrins Choose Their Möbius/Hückel Aromatic Topology

(2010) Jong Min Lim et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Revealing Noncovalent Interactions

(2010) Erin R. Johnson et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Conformational Changes ofmeso-Aryl Substituted Expanded Porphyrins upon Protonation: Effects on Photophysical Properties and Aromaticity

(2009) Jae-Yoon Shin et al.   JOURNAL OF PHYSICAL CHEMISTRY B

Universal Solvation Model Based on Solute Electron Density and on a Continuum Model of the Solvent Defined by the Bulk Dielectric Constant and Atomic Surface Tensions

(2009) Aleksandr V. Marenich et al.   JOURNAL OF PHYSICAL CHEMISTRY B

Macrocyclic aromaticity in Hückel and Möbius conformers of porphyrinoids

(2009) Jun-ichi Aihara et al.   ORGANIC & BIOMOLECULAR CHEMISTRY

Substituent effects on the aromaticity of carbocyclic five-membered rings

(2009) Mercedes Alonso et al.   PHYSICAL CHEMISTRY CHEMICAL PHYSICS

Protonation-Triggered Conformational Changes to Möbius Aromatic [32]Heptaphyrins(1.1.1.1.1.1.1)

(2008) Shohei Saito et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

The photophysical properties of expanded porphyrins: relationships between aromaticity, molecular geometry and non-linear optical properties

(2008) Jong Min Lim et al.   CHEMICAL COMMUNICATIONS

Macrocyclic Conjugation Pathways in Porphyrins

(2008) Jun-ichi Aihara   JOURNAL OF PHYSICAL CHEMISTRY A

Intrinsically Chiral Aromaticity. Rules Incorporating Linking Number, Twist, and Writhe for Higher-Twist Möbius Annulenes

(2008) Shay M. Rappaport et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Metalation of Expanded Porphyrins: A Chemical Trigger Used To Produce Molecular Twisting and Möbius Aromaticity

(2007) Yasuo Tanaka et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION