Assessment of the performance of six indices in predicating the aromaticity of planar porphyrinoids

[1] Lin S(2015)Covalent organic frameworks comprising cobalt porphyrins for catalytic CO(2) reduction in water Science 349 1208-1213

[2] Diercks CS(2020)Understanding the structures and aromaticity of heteroporphyrins with computations Org Biomol Chem 84 274-284

[3] Zhang YB(2002)Unsaturated macrocyclic compounds. XXIII.1 The synthesis of the fully conjugated macrocyclic polyenes cycloöctadecanonaene ([18]annulene),2 cyclotetracosadodecaene ([24]Annulene), and cyclotriacontapentadecaene ([30]Annulene) J Am Chem Soc 65 143-152

[4] Kornienko N(1993)The porphyrins from the ‘annulene chemist’s’ perspective Pure Appl Chem 29 e202202264-2796

[5] Nichols EM(2023)Quest for the most aromatic pathway in charged expanded porphyrins Chemistry 20 2787-4340

[6] Zhao Y(2018)New electron delocalization tools to describe the aromaticity in porphyrinoids Phys Chem Phys 50 4288-11730

[7] Paris AR(2011)Figure eights, Mobius bands, and more: conformation and aromaticity of porphyrinoids Angew Chem Int Ed Engl 116 11718-321

[8] Kim D(2012)Validity and limitations of the bridged annulene model for porphyrins J Phys Chem A 135 315-21274

[9] Yang P(2013)Description of aromaticity in porphyrinoids J Am Chem Soc 22 21267-3414

[10] Yaghi OM(2020)Local and macrocyclic (anti)aromaticity of porphyrinoids revealed by the topology of the induced magnetic field Phys Chem Chem Phys 77 3408-6150

[1] Lin S(2015)Covalent organic frameworks comprising cobalt porphyrins for catalytic CO(2) reduction in water Science 349 1208-1213

[2] Diercks CS(2020)Understanding the structures and aromaticity of heteroporphyrins with computations Org Biomol Chem 84 274-284

[3] Zhang YB(2002)Unsaturated macrocyclic compounds. XXIII.1 The synthesis of the fully conjugated macrocyclic polyenes cycloöctadecanonaene ([18]annulene),2 cyclotetracosadodecaene ([24]Annulene), and cyclotriacontapentadecaene ([30]Annulene) J Am Chem Soc 65 143-152

[4] Kornienko N(1993)The porphyrins from the ‘annulene chemist’s’ perspective Pure Appl Chem 29 e202202264-2796

[5] Nichols EM(2023)Quest for the most aromatic pathway in charged expanded porphyrins Chemistry 20 2787-4340

[6] Zhao Y(2018)New electron delocalization tools to describe the aromaticity in porphyrinoids Phys Chem Phys 50 4288-11730

[7] Paris AR(2011)Figure eights, Mobius bands, and more: conformation and aromaticity of porphyrinoids Angew Chem Int Ed Engl 116 11718-321

[8] Kim D(2012)Validity and limitations of the bridged annulene model for porphyrins J Phys Chem A 135 315-21274

[9] Yang P(2013)Description of aromaticity in porphyrinoids J Am Chem Soc 22 21267-3414

[10] Yaghi OM(2020)Local and macrocyclic (anti)aromaticity of porphyrinoids revealed by the topology of the induced magnetic field Phys Chem Chem Phys 77 3408-6150