Search Results - "MORGAN, Brad P"

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  1. 1

    Sterically Encumbered Bipyridyl-Derivatized Conjugated Polymers and Metallopolymers Incorporating Phenylenevinylene, Phenyleneethynylene, and Fluorenylene Segments by He, Susan, Buelt, Ashley A, Hanley, Jessica M, Morgan, Brad P, Tennyson, Andrew G, Smith, Rhett C

    Published in Macromolecules (28-08-2012)
    “…This work reports the preparation of a series of 2,2′-bipyridyl (bipy) modified π-conjugated polymers having an average of one or three monomer units…”
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    Journal Article
  2. 2

    Poly(p‐phenylene ethynylene) Incorporating Sterically Enshrouding m‐Terphenyl Oxacyclophane Canopies by Morgan, Brad P., Gilliard, Robert J., Loungani, Rahul S., Smith, Rhett C.

    Published in Macromolecular rapid communications. (18-08-2009)
    “…A sterically encumbered m‐terphenyl oxacyclophane substituted with two aryl iodide substituents has been prepared as a versatile monomer for the preparation of…”
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    Journal Article
  3. 3

    Dizinc Enzyme Model/Complexometric Indicator Pairs in Indicator Displacement Assays for Inorganic Phosphates under Physiological Conditions by Morgan, Brad P, He, Susan, Smith, Rhett C

    Published in Inorganic chemistry (29-10-2007)
    “…A dizinc phosphohydrolase enzyme model complex employing the dinucleating ligand 2,6-bis-[(bis-pyridin-2-ylmethyl-amino)methyl]-4-methylphenol (L1) was tested…”
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    Journal Article
  4. 4

    Conjugated Polymers Featuring Oxacyclophane-Scaffolded π-Stacking Interactions by Mangalum, Anshuman, Morgan, Brad P., Tennyson, Andrew G., Smith, Rhett C.

    Published in Macromolecular chemistry and physics (01-02-2014)
    “…An oxacyclophane framework is modified to include π‐conjugated segments positioned so as to allow an optimized face‐to‐face π‐stacking interaction between…”
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    Journal Article
  5. 5
  6. 6

    Poly(p-phenylenevinylene) Derivatives with Defined Conjugation Segments and Post-Polymerization Modification with Sterically Enshrouded Chromophores by Buelt, Ashley A., Colberg, Allison J., Dennis, Ashlyn E., Jecen, Kristine M., Morgan, Brad P., Smith, Rhett C.

    Published in Macromolecular rapid communications. (20-04-2010)
    “…Two poly(p‐phenylenevinylene) derivative alternating copolymers (P1‐I and P2‐I) have been prepared featuring iodo substituents and m‐phenylene units to…”
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    Journal Article
  7. 7

    Macromol. Rapid Commun. 16/2009 by Morgan, Brad P., Gilliard Jr, Robert J., Loungani, Rahul S., Smith, Rhett C.

    Published in Macromolecular rapid communications. (18-08-2009)
    “…Back Cover: A macrocyclic monomer that provides a steric canopy over one face of the appended aryl ring is prepared and a poly(p‐phenylene ethynylene)…”
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    Journal Article
  8. 8

    Wide bite angle diphosphine rhodium complexes: Synthesis, structure, and catalytic 1,4-addition of arylboronic acids to enones by Morgan, Brad P., Smith, Rhett C.

    “…A terphspan Rh(I) complex has been prepared and structurally characterized. The terphspan ligand L1 has a wide bite angle of 171.37° in the [ClRh(CO) L1]…”
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    Journal Article
  9. 9

    Conjugated Polymers Featuring Oxacyclophane-Scaffolded [pi]-Stacking Interactions by Mangalum, Anshuman, Morgan, Brad P, Tennyson, Andrew G, Smith, Rhett C

    Published in Macromolecular chemistry and physics (01-02-2014)
    “…An oxacyclophane framework is modified to include π-conjugated segments positioned so as to allow an optimized face-to-face π-stacking interaction between…”
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    Journal Article
  10. 10
  11. 11

    Synthesis of meta-terphenyl scaffolded molecules for catalysis and sensor applications by Morgan, Brad P

    Published 01-01-2010
    “…The utility of the m-terphenyl has been observed in a wide variety of applications since its first discovery. The tunable conformational flexibility…”
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    Dissertation
  12. 12

    Synthesis of meta-terphenyl scaffolded molecules for catalysis and sensor applications by Morgan, Brad P

    “…The utility of the m-terphenyl has been observed in a wide variety of applications since its first discovery. The tunable conformational flexibility…”
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    Dissertation