3433 - 3435 |
Introduction: Delocalization - Pi and Sigma Schleyer PV |
3436 - 3447 |
Crocker, not Armit and Robinson, Begat the six aromatic electrons Balaban AT, Schleyer PV, Rzepa HS |
3448 - 3481 |
Conjugated polymers and aromaticity Kertesz M, Choi CH, Yang SJ |
3482 - 3512 |
Sigma- and Pi-electron delocalization: Focus on substituent effects Krygowski TM, Stepien BT |
3513 - 3560 |
Interrelation between H-bond and Pi-electron delocalization Sobczyk L, Grabowski SJ, Krygowski TM |
3561 - 3612 |
Tautomeric equilibria in relation to Pi-electron delocalization Raczynska ED, Kosinska W, Osmialowski B, Gawinecki R |
3613 - 3642 |
Spherical aromaticity: Recent work on fullerenes, polyhedral boranes, and related structures Chen ZF, King RB |
3643 - 3696 |
Curved Pi-conjugation, aromaticity, and the related chemistry of small fullerenes (< C-60) and single-walled carbon nanotubes Lu X, Chen ZF |
3697 - 3715 |
Mobius aromaticity and delocalization Rzepa HS |
3716 - 3757 |
All-metal aromaticity and antiaromaticity Boldyrev AI, Wang LS |
3758 - 3772 |
Anisotropy of the induced current density (ACID), a general method to quantify and visualize electronic delocalization Geuenich D, Hess K, Kohler F, Herges R |
3773 - 3811 |
Energetic aspects of cyclic Pi-electron delocalization: Evaluation of the methods of estimating aromatic stabilization energies Cyranski MK |
3812 - 3841 |
Description of electron delocalization via the analysis of molecular fields Merino G, Vela A, Heine T |
3842 - 3888 |
Nucleus-independent chemical shifts (NICS) as an aromaticity criterion Chen ZF, Wannere CS, Corminboeuf C, Puchta R, Schleyer PV |
3889 - 3910 |
The magnetic shielding function of molecules and Pi-electron delocalization Heine T, Corminboeuf C, Seifert G |
3911 - 3947 |
Theoretical evaluation of electron delocalization in aromatic molecules by means of atoms in molecules (AIM) and electron localization function (ELF) topological approaches Poater J, Duran M, Sola M, Silvi B |