Design of bridged polycyclic diolefin precursors for prismanes using FMO order as criteria. Interbridge distance as a new factor for controlling the intramolecular [π2 + π2] cycloaddition
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry
Reference24 articles.
1. Strain, orbital interaction, and conformation of propella[34]prismane and its precursor diolefin
2. Analysis of the interactions responsible for long-range through-bond-mediated electronic coupling between remote chromophores attached to rigid polynorbornyl bridges
Cited by 16 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Synthesis, structure, and photoreactions of fluorinated 2,11-diaza[32 ]paracyclophane: Photochemical formation of cage-diene type benzene dimer;Journal of Physical Organic Chemistry;2017-07-05
2. ChemInform Abstract: Design of Bridged Polycyclic Diolefin Precursors for Prismanes Using FMO Order as Criteria. Interbridge Distance as a New Factor for Controlling the Intramolecular (π2 + π2) Cycloaddition.;ChemInform;2010-08-19
3. Chemistry of Cubane and Other Prismanes;PATAI'S Chemistry of Functional Groups;2009-12-15
4. Photochemistry of Nitrogen-Bridged Cyclophanes: 2,11-Diaza[32]anthracenoparacyclophane and 2,11-Diaza[32]paracyclophane Systems;Synlett;2008-07-15
5. Photochemical Study of [33](1,3,5)Cyclophane and Emission Spectral Properties of [3n]Cyclophanes (n = 2−6);Journal of the American Chemical Society;2004-09-30
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