2026-09-20T15:34:42Z https://www.ideals.illinois.edu/oai-pmh

oai:www.ideals.illinois.edu:2142/84133 2023-07-11 col_2142_5131 col_2142_14789 com_2142_5130 com_2142_14788 com_2142_8903

Moore, Jeffrey S. Zimmerman, Steven C. Zimmerman, Ned Walter 2015-09-25T22:13:06Z 2015-09-25T22:13:06Z 10000-01-01 2003 2003 In the second investigation, the use of multiple highly directional hydrogen bonds for the formation of supramolecular polymers was explored. Synthetic routes toward supramolecular polymer end-groups based upon the 2-amino-5-deazapterin and 2,7-diamino-[1,8]-naphthyridine ring systems were pursued. While it was found that the end-groups could be made, the synthetic difficulties and inefficiencies encountered precluded the isolation of sufficient sample quantities for the exploration of the materials' properties. The further development of end-groups based upon these ring systems was discontinued. Made available in DSpace on 2015-09-25T22:13:06Z (GMT). No. of bitstreams: 2 license.txt: 4848 bytes, checksum: 96035ab3f5e1c23cc7138a224ce498bd (MD5) 3111667.pdf: 7971071 bytes, checksum: 6fda5803b07baf00cfc637d6e90d756a (MD5) Previous issue date: 2003 Embargo set by: Seth Robbins for item 85414 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs U of I Only 138 p. Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2003. http://hdl.handle.net/2142/84133 (MiAaPQ)AAI3111667 eng Chemistry, Organic Explorations in Supramolecular Chemistry: Part 1. Development of a Modular System for the Study of Self-Organization Through Microphase Segregation in Discotic Liquid Crystals. Part 2. Investigation of Deazapterins and Naphthyridines as End-Groups for Supramolecular Polymers text Chemisty Chemisty University of Illinois at Urbana-Champaign Dissertation Ph.D.