Discrimination of pseudo-meta and pseudo-para diamino-octafluoro[2.2]paracyclophanes by 1 H, 19 F, and 13 C NMR-Reference-Cited by-同舟云学术

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Discrimination of pseudo-meta and pseudo-para diamino-octafluoro[2.2]paracyclophanes by 1 H, 19 F, and 13 C NMR

Published:2012-11-20 Issue:12 Volume:50 Page:809-812
ISSN:0749-1581
Container-title:Magnetic Resonance in Chemistry
language:en
Short-container-title:Magn. Reson. Chem.

Author:

Roche Alex J.¹,Marchione Alexander A.²

Affiliation:

1. Department of Chemistry, Rutgers; The State University of New Jersey; Camden NJ USA

2. DuPont Central Research and Development; Experimental Station; Wilmington DE USA

Funder

National Science Foundation

Publisher

Wiley

Subject

General Materials Science,General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mrc.3882/fullpdf

Reference31 articles.

1. Synthesis of medio- and macrocyclic compounds by high dilution principle techniques

2. The electronic structure of cyclophanes as suggested by their photoelectron spectra

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1. Molecular Insights into [2.2]Paracyclophane‐Based Functional Materials: Chemical Aspects Behind Functions;Advanced Functional Materials;2024-04-15

2. Palladium catalyzed cross- and homo-coupling reactions of 4-Halo-1,1,2,2,9,9,10,10-octafluoro[2.2]paracyclophanes with various organometallic reagents;Journal of Fluorine Chemistry;2015-07

3. Chapter 5. Applications of spin–spin couplings;Nuclear Magnetic Resonance;2014

4. Efficient NMR enantiodiscrimination of bridge fluorinated paracyclophanes using lanthanide tris β-diketonate complexes;Tetrahedron: Asymmetry;2013-11

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