Global Aromaticity at the Nanoscale

[1]  H. Anderson,et al.  Global Aromaticity and Antiaromaticity in Porphyrin Nanoring Anions† , 2019, Angewandte Chemie.

[2]  L. Herz,et al.  Tuning the Circumference of Six-Porphyrin Nanorings , 2019, Journal of the American Chemical Society.

[3]  J. Cybińska,et al.  Lemniscular [16]Cycloparaphenylene: A Radially Conjugated Figure-Eight Aromatic Molecule. , 2019, Journal of the American Chemical Society.

[4]  L. Herz,et al.  Aromaticity and Antiaromaticity in the Excited States of Porphyrin Nanorings , 2019, The journal of physical chemistry letters.

[5]  V. Lynch,et al.  Three-Dimensional Fully Conjugated Carbaporphyrin Cage. , 2018, Journal of the American Chemical Society.

[6]  A. Osuka,et al.  Quadruply Twisted Hückel-Aromatic Dodecaphyrin. , 2018, Angewandte Chemie.

[7]  M. Wasielewski,et al.  Fully Conjugated [4]Chrysaorene. Redox-Coupled Anion Binding in a Tetraradicaloid Macrocycle. , 2018, Journal of the American Chemical Society.

[8]  T. Herng,et al.  Global Aromaticity in Macrocyclic Cyclopenta-Fused Tetraphenanthrenylene Tetraradicaloid and Its Charged Species. , 2018, Angewandte Chemie.

[9]  T. Herng,et al.  Macrocyclic Polyradicaloids with Unusual Super-ring Structure and Global Aromaticity , 2018, Chem.

[10]  T. Herng,et al.  From Open-Shell Singlet Diradicaloid to Closed-Shell Global Antiaromatic Macrocycles. , 2018, Angewandte Chemie.

[11]  Lukas N. Wirz,et al.  Magnetically Induced Ring-Current Strengths in Möbius Twisted Annulenes , 2018, The journal of physical chemistry letters.

[12]  H. Anderson,et al.  Single-Acetylene Linked Porphyrin Nanorings , 2017, Journal of the American Chemical Society.

[13]  T. Herng,et al.  Fluorenyl Based Macrocyclic Polyradicaloids. , 2017, Journal of the American Chemical Society.

[14]  T. K. Chandrashekar,et al.  Bicyclic Baird-type aromaticity. , 2017, Nature chemistry.

[15]  H. Anderson,et al.  Aromatic and antiaromatic ring currents in a molecular nanoring , 2016, Nature.

[16]  S. Neya,et al.  [62]Tetradecaphyrin and Its Mono- and Bis-Zn(II) Complexes. , 2016, Chemistry.

[17]  Rebecca L. M. Gieseking,et al.  Benchmarking Density Functional Theory Approaches for the Description of Symmetry Breaking in Long Polymethine Dyes , 2016 .

[18]  Renana Gershoni‐Poranne,et al.  Magnetic criteria of aromaticity. , 2015, Chemical Society reviews.

[19]  Woojae Kim,et al.  Stable [48]-, [50]-, and [52]dodecaphyrins(1.1.0.1.1.0.1.1.0.1.1.0): the largest Hückel aromatic molecules. , 2015, Chemistry.

[20]  M. Malfois,et al.  Vernier-Templated Synthesis, Crystal Structure, and Supramolecular Chemistry of a 12-Porphyrin Nanoring , 2014, Chemistry.

[21]  R. Herges,et al.  Möbius molecules with twists and writhes. , 2013, Chemical communications.

[22]  C. Lambert,et al.  Organic mixed-valence compounds: a playground for electrons and holes. , 2012, Angewandte Chemie.

[23]  M. Stępień,et al.  Figure eights, Möbius bands, and more: conformation and aromaticity of porphyrinoids. , 2011, Angewandte Chemie.

[24]  M. Malfois,et al.  Vernier templating and synthesis of a 12-porphyrin nano-ring , 2011, Nature.

[25]  P. Edwards,et al.  ‘… a metal conducts and a non-metal doesn't’ , 2010, Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences.

[26]  Giovanni Scalmani,et al.  Can short-range hybrids describe long-range-dependent properties? , 2009, The Journal of chemical physics.

[27]  H. Rzepa,et al.  Intrinsically chiral aromaticity. Rules incorporating linking number, twist, and writhe for higher-twist Möbius annulenes. , 2008, Journal of the American Chemical Society.

[28]  Rainer Herges,et al.  Topology in chemistry: designing Möbius molecules. , 2006, Chemical reviews.

[29]  Michael M Haley,et al.  Renaissance of annulene chemistry. , 2006, Chemical reviews.

[30]  Clémence Corminboeuf,et al.  Nucleus-independent chemical shifts (NICS) as an aromaticity criterion. , 2005, Chemical reviews.

[31]  G. Burley.  Trannulenes with "in-plane" aromaticity: candidates for harvesting light energy. , 2005, Angewandte Chemie.

[32]  R. J. Luyken,et al.  Spectroscopy of nanoscopic semiconductor rings. , 1999, Physical review letters.

[33]  Paul von Ragué Schleyer,et al.  From Dodecahedrapentaene to the “[n]Trannulenes”. A New In-Plane Aromatic Family , 1998 .

[34]  Laren M. Tolbert,et al.  Beyond the Cyanine Limit: Peierls Distortion and Symmetry Collapse in a Polymethine Dye , 1997 .

[35]  M. Frisch,et al.  Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Force Fields , 1994 .

[36]  F. B. Fuller.  The writhing number of a space curve. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[37]  E. Hückel,et al.  Quantentheoretische Beiträge zum Benzolproblem , 1931 .