Cycloparaphenylenes (CPPs) represent the unit-cycles of conductive armchair carbon nanotubes (CNTs). In addition to their utility for the bottom-up synthesis of CNTs with discrete diameter and chirality, these strained hydrocarbon macrocycles have attractive properties of their own for material science and organic electronics. Herein I report research focused on advancing the synthetic technology behind CPPs, culminating in the synthesis of [5]CPP, the smallest and most highly-strained member of the CPP series to date, as well as the derivitization of the CPP platform to include chiral nanohoops with a spiral carbon backbone and photoswitchable nanohoops based on azobenzene incorporation into the CPP architecture.
The synthesis and characterization of [5]CPP, 1,5-naphthyl[6]CPP, azo[11]CPP, and azo[9]CPP are reported along with advanced intermediates towards rotationally restricted 2,6-naphthyl[6]CPP and preliminary photoisomerization results for azo[11]CPP and azo[9]CPP.
This dissertation contains both previously published and unpublished co-authored material.
| Identifer | oai:union.ndltd.org:uoregon.edu/oai:scholarsbank.uoregon.edu:1794/19282 |
| Date | 18 August 2015 |
| Creators | Evans, Paul |
| Contributors | Tyler, David |
| Publisher | University of Oregon |
| Source Sets | University of Oregon |
| Language | en_US |
| Detected Language | English |
| Type | Electronic Thesis or Dissertation |
| Rights | All Rights Reserved. |
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