Negatively curved molecular nanocarbons containing multiple heptagons are enabled by the Scholl reactions of macrocyclic precursors

[1]  Jianbin Xu,et al.  Robust Radical Cations of Hexabenzoperylene Exhibiting High Conductivity and Enabling an Organic Nonvolatile Optoelectronic Memory. , 2022, Journal of the American Chemical Society.

[2]  Q. Miao,et al.  The Scholl Reaction as a Powerful Tool for Synthesis of Curved Polycyclic Aromatics. , 2022, Chemical reviews.

[3]  N. Martín,et al.  Synthetic chiral molecular nanographenes: the key figure of the racemization barrier. , 2022, Chemical communications.

[4]  Saleh A. Ahmed,et al.  Scholl reaction as a powerful tool for the synthesis of nanographenes: a systematic review , 2021, RSC advances.

[5]  Ying Wang,et al.  Charging a Negatively Curved Nanographene and Its Covalent Network. , 2021, Journal of the American Chemical Society.

[6]  Zeming Xia,et al.  Synthesis of Zigzag Carbon Nanobelts through Scholl Reactions. , 2021, Angewandte Chemie.

[7]  K. Yonekura,et al.  Double-Helix Supramolecular Nanofibers Assembled from Negatively Curved Nanographenes. , 2020, Journal of the American Chemical Society.

[8]  K. Müllen,et al.  Negatively Curved Nanographene with Heptagonal and [5]Helicene Units , 2020, Journal of the American Chemical Society.

[9]  K. Takasu,et al.  Helical Nanographenes Embedded with Contiguous Azulene Units. , 2020, Journal of the American Chemical Society.

[10]  Zhifeng Liu,et al.  An 80-Carbon Aromatic Saddle Enabled by a Naphthalene-Directed Scholl Reaction , 2020, Organic Materials.

[11]  A. Stanger.  NICS - Past and Present , 2020 .

[12]  H. Klauk,et al.  2,7,11,16‐Tetra‐tert‐Butyl Tetraindenopyrene Revisited by an “Inverse” Synthetic Approach , 2020, Chemistry.

[13]  D. Gryko,et al.  Synthetic Applications of Oxidative Aromatic Coupling—From Biphenols to Nanographenes , 2019, Angewandte Chemie.

[14]  F. Rominger,et al.  A Chiral Polycyclic Aromatic Hydrocarbon Monkey Saddle , 2019, Angewandte Chemie.

[15]  Xuan Yang,et al.  Contorted Polycyclic Aromatic Hydrocarbons with Two Embedded Azulene Units , 2019, Angewandte Chemie.

[16]  Zhifeng Liu,et al.  Synthesis, Structures, and Properties of Heptabenzo[7]circulene and Octabenzo[8]circulene. , 2019, Journal of the American Chemical Society.

[17]  M. Stępień,et al.  Bowls, Hoops, and Saddles: Synthetic Approaches to Curved Aromatic Molecules. , 2018, Angewandte Chemie.

[18]  N. Martín,et al.  π-Extended Corannulene-Based Nanographenes: Selective Formation of Negative Curvature. , 2018, Journal of the American Chemical Society.

[19]  Yongjin Lee,et al.  Generating carbon schwarzites via zeolite-templating , 2018, Proceedings of the National Academy of Sciences.

[20]  Q. Miao,et al.  Toward Negatively Curved Carbons. , 2018, Accounts of chemical research.

[21]  Jianbin Xu,et al.  Functionalized π Stacks of Hexabenzoperylenes as a Platform for Chemical and Biological Sensing , 2018, Chem.

[22]  Zhifeng Liu,et al.  A Twisted Nanographene Consisting of 96 Carbon Atoms. , 2017, Angewandte Chemie.

[23]  Zhifeng Liu,et al.  Synthesis, Structure, and Properties of Tetrabenzo[7]circulene. , 2017, Organic letters.

[24]  M. Mayor,et al.  Chirality in curved polyaromatic systems. , 2017, Chemical Society reviews.

[25]  Jung-Ki Park,et al.  Lanthanum-catalysed synthesis of microporous 3D graphene-like carbons in a zeolite template , 2016, Nature.

[26]  M. Hatanaka.  Puckering Energetics and Optical Activities of [7]Circulene Conformers. , 2016, The journal of physical chemistry. A.

[27]  Kenichiro Itami,et al.  Synthesis, Structures, and Properties of π-Extended Double Helicene: A Combination of Planar and Nonplanar π-Systems. , 2015, Journal of the American Chemical Society.

[28]  Jianbin Xu,et al.  Monolayer Field‐Effect Transistors of Nonplanar Organic Semiconductors with Brickwork Arrangement , 2015, Advanced materials.

[29]  Xiaomin Xu,et al.  Aromatic saddles containing two heptagons. , 2015, Journal of the American Chemical Society.

[30]  Severin T. Schneebeli,et al.  Synthesis and structural data of tetrabenzo[8]circulene. , 2014, Chemistry.

[31]  Toshiyasu Suzuki,et al.  Tetrabenzo[8]circulene: aromatic saddles from negatively curved graphene. , 2013, Journal of the American Chemical Society.

[32]  L. T. Scott,et al.  A grossly warped nanographene and the consequences of multiple odd-membered-ring defects. , 2013, Nature chemistry.

[33]  M. Kuo,et al.  Synthesis, structural analysis, and properties of [8]circulenes. , 2013, Angewandte Chemie.

[34]  H. Bock,et al.  Twisted polycyclic arenes by intramolecular Scholl reactions of C3-symmetric precursors. , 2013, The Journal of organic chemistry.

[35]  Xiaomin Xu,et al.  Curved polycyclic aromatic molecules that are π-isoelectronic to hexabenzocoronene. , 2012, Journal of the American Chemical Society.

[36]  F. Wudl,et al.  Synthesis and structure characterization of a stable nonatwistacene. , 2012, Angewandte Chemie.

[37]  Wei Li,et al.  Electrochemical Considerations for Determining Absolute Frontier Orbital Energy Levels of Conjugated Polymers for Solar Cell Applications , 2011, Advanced materials.

[38]  D. Tománek,et al.  Designing rigid carbon foams , 2009, Journal of physics. Condensed matter : an Institute of Physics journal.

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

[40]  G. Portella,et al.  Local aromaticity of [n]acenes, [n]phenacenes, and [n]helicenes (n = 1-9). , 2005, The Journal of organic chemistry.

[41]  J. Ihm,et al.  Magnetism in all-carbon nanostructures with negative Gaussian curvature. , 2003, Physical review letters.

[42]  T. M. Krygowski,et al.  Structural aspects of aromaticity. , 2001, Chemical reviews.

[43]  Koji Yamamoto,et al.  [7.7]Circulene, a Molecule Shaped Like a Figure of Eight , 1991 .

[44]  A. Mackay,et al.  Diamond from graphite , 1991, Nature.

[45]  Y. Kai,et al.  Synthesis and molecular structure of [7]circulene , 1988 .

[46]  Y. Kai,et al.  Synthesis and characterization of [7]circulene , 1983 .

[47]  Robert A Pascal,et al.  Twisted acenes. , 2006, Chemical reviews.

[48]  T. M. Krygowski,et al.  Definition of aromaticity basing on the harmonic oscillator model , 1972 .