Experimental and Theoretical Studies on Constitutional Isomers of 2,6-Dihydroxynaphthalene Carbaldehydes. Effects of Resonance-Assisted Hydrogen Bonding on the Electronic Absorption Spectra-Reference-Cited by-同舟云学术

Experimental and Theoretical Studies on Constitutional Isomers of 2,6-Dihydroxynaphthalene Carbaldehydes. Effects of Resonance-Assisted Hydrogen Bonding on the Electronic Absorption Spectra

Published:2008-12-04 Issue:2 Volume:74 Page:520-529
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Houjou Hirohiko¹,Motoyama Takatoshi¹,Banno Seisaku¹,Yoshikawa Isao¹,Araki Koji¹

Affiliation:

1. Institute of Industrial Science, University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8505, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo802345f

Reference85 articles.

1. Selective Inclusion of a Hetero-Guest Pair in a Molecular Host: Formation of Stable Charge-Transfer Complexes in Cucurbit[8]uril

2. Molecular Loop Lock: A Redox-Driven Molecular Machine Based on a Host-Stabilized Charge-Transfer Complex

3. Unprecedented host-induced intramolecular charge-transfer complex formationElectronic supplementary information (ESI) available: synthetic procedure and characterization data of 1 and 2. See http://www.rsc.org/suppdata/cc/b2/b208280b/

4. The Synthesis and Spectroscopic Properties of Macrocyclic Polyethers Containing Two Different Aromatic Moieties and Their [2]Catenanes Incorporating Cyclobis(paraquat-p-phenylene)

5. Spontaneous Colorimetric Sensing of the Positional Isomers of Dihydroxynaphthalene in a 1D Organogel Matrix

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