Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Synthetic polymers and methods of making and using the same

Patent ·
OSTI ID:1257357
Monomer embodiments that can be used to make polymers, such as homopolymers, heteropolymers, and that can be used in particular embodiments to make sequence-defined polymers are described. Also described are methods of making polymers using such monomer embodiments. Methods of using the polymers also are described.
Research Organization:
Pacific Northwest National Laboratory (PNNL), Richland, WA (United States)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
Assignee:
Battelle Memorial Institute (Richland, WA)
Patent Number(s):
9,365,676
Application Number:
14/556,021
OSTI ID:
1257357
Country of Publication:
United States
Language:
English

References (21)

Elegant Chemistry to Directly Anchor Intact Saccharides on Solid Surfaces Used for the Fabrication of Bioactivity-Conserved Saccharide Microarrays journal May 2012
Fluorescent Cellulose Microfibrils As Substrate for the Detection of Cellulase Activity journal May 2003
The use of triazine polymer as a structurized sorbent for chromatography journal April 2013
Synthesis and conformational studies of pseudopeptides containing an unsymmetrical triazine scaffold journal May 2008
Linear polymers containing the 1,3,5-triazine nucleus journal October 1959
Preparation of Microporous Polymers Based on 1,3,5-Triazine Units Showing High CO2 Adsorption Capacity journal May 2012
Functional conjugated microporous polymers: from 1,3,5-benzene to 1,3,5-triazine journal January 2012
Pseudo porphyrinyl amino acids based on 1,3,5-triazine scaffold: new tools for the synthesis of peptidic porphyrins journal June 2011
Synthesis, structural investigation and computational modelling of water-binding aquafoldamers journal January 2012
Reactive Dyes in the Coloration of Cellulosic Materials journal January 1969
Self-Complementarity Achieved through Quadruple Hydrogen Bonding journal February 1998
Synthesis and characterization of a new hyperbranched organic–inorganic solid polymer electrolyte with cyanuric chloride as a core element journal October 2011
Helicity-Encoded Molecular Strands: Efficient Access by the Hydrazone Route and Structural Features journal May 2003
Synthesis of polyguanamines from 2-N,N-dibutylamino-4,6-dichloro-1,3,5-triazine with aromatic diamines journal May 2013
The Reactions of Cold-dyeing Procion Dyes with Cellulose journal April 1960
Recent applications of 2,4,6-trichloro-1,3,5-triazine and its derivatives in organic synthesis journal October 2006
2-Alkyl-4,6-dialkylamino-1,3,5-triazines via Grignard Alkylation of Cyanuric Chloride: An Aged Reaction Revisited journal December 2000
Synthesis, characterization and antibacterial activity of new fluorescent chitosan derivatives journal April 2014
Duplex Oligomers Defined via Covalent Casting of a One-Dimensional Hydrogen-Bonding Motif journal May 2002
Refolding Foldamers: Triazene-Arylene Oligomers That Change Shape with Chemical Stimuli journal September 2007
The 8 year thicket of triazine dendrimers: strategies, targets and applications
  • Simanek, E. E.; Abdou, H.; Lalwani, S.
  • Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences, Vol. 466, Issue 2117, p. 1445-1468 https://doi.org/10.1098/rspa.2009.0108
journal May 2009