Molecular Conductors Based on Axially Substituted Phthalocyanine Neutral Radicals
Author:
Affiliation:
1. a Department of Chemistry, Faculty of Science , Hokkaido University , Sapporo , 060 , Japan
Publisher
Informa UK Limited
Subject
Condensed Matter Physics
Link
https://www.tandfonline.com/doi/pdf/10.1080/10587259608037931
Reference9 articles.
1. Crystal Structure of the Electrochemical Product of Potassium Dicyanophthalocyaninatocobalt(III). Novel Two-Dimensional Stacking Interaction of Phthalocyanine
2. Multi-Dimensional Stacking Structures in Phthalocyanine-Based Electrical Conductors, K[Co(phthalocyaninato)(CN)2]2·5CH3CN and Co(phthalocyaninato)(CN)2·2H2O
3. Design of Two-Dimensional Stacking Structures: Twin-Type Molecules and Steric Interaction of Axial Substituents
4. Approaches to controlling the dimensionality in molecular conductors. Axially substituted phthalocyanines and twin-type molecules
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1. Formation of Three-Dimensional Electronic Networks Using Axially Ligated Metal Phthalocyanines as Stable Neutral Radicals;Crystals;2020-08-24
2. Cyanometallates as Halogen Bond Acceptors;Crystal Growth & Design;2011-12-16
3. PhthalocyaninesVersatile Components of Molecular Conductors;Chemical Reviews;2004-09-16
4. Single-Crystal Structures of Phthalocyanine Complexes and Related Macrocycles;The Porphyrin Handbook;2003
5. Novel phthalocyanine‐based conductors: tunable Π–Π stacking structure through the steric and chemical interactions of axial ligands;Journal of Porphyrins and Phthalocyanines;2001-01
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