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Jennifer M Heemstra

Publications and source records attributed to Jennifer M Heemstra.

5 recordsLinked to original sources
PubMed2004

Enhanced methylation rate within a foldable molecular receptor.

A N,N-(dimethylamino)pyridine monomer is incorporated into the backbone of a m-phenyleneethynylene oligomer such that the pyridine nitrogen is located on the interior surface of the binding cavity in the folded structure of the oligomer. For an oligomer having a chain length of 13 monomer units, competitive inhibition experiments reveal that methyl iodide binds weakly within the oligomer cavity with an association constant K(a) = 2 M(-1), and the oligomer-methyl iodide complex reacts with unimolecular rate constant k(u) = 0.082 s(-1) to provide the methylated product. The effective molarity is calculated to be 230 M by comparison of k(u) for the 13-mer with the second-order rate constant for a 3-mer that is too short to fold and thus unable to bind methyl iodide.

Journal Article↗
PubMed2004

Single-site modifications and their effect on the folding stability of m-phenylene ethynylene oligomers.

[reaction: see text] The folded structure of a m-phenylene ethynylene oligomer is tolerant to single-site modifications to both the backbone sequence and end groups. The helical structure is reinforced by multiple noncovalent interactions, allowing the oligomer sequence to be customized without a significant change in stability in most cases. The small changes that are observed are consistent with the expected behavior of pi-stacked systems and demonstrate subtle control over folding through single-site modifications.

Journal Article↗
PubMed2004

Pyridine-containing m-phenylene ethynylene oligomers having tunable basicities.

Incorporation of a pyridine monomer into the backbone of a m-phenylene ethynylene oligomer allows functionalization of the interior binding cavity of the folded oligomer. The basicity of the inwardly directed pyridine moiety was modulated by changing the substituents on the pyridine ring and through oligomer folding, granting access to a pK(a) range of 5-14 in acetonitrile. [reaction: see text]

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PubMed2004

Folding-promoted methylation of a helical DMAP analogue.

The methylation rate for a series of pyridine-containing phenylene ethynylene oligomers shows a nonlinear dependence on chain length, with a significant rate enhancement observed for oligomers that adopt a folded, helical conformation. The folded structure provides a microenvironment that lowers the energy barrier for the methylation reaction. Of these noncovalent interactions, the largest stabilization may arise from binding of methyl iodide in the hydrophobic cavity of the folded oligomer, in close proximity to the pyridine nucleophile.

Journal Article↗