Fully amorphous atactic and isotactic block copolymers and their self-assembly into nano- and microscopic vesicles

<p>Data underlying the figures in the publication &ldquo;Fully amorphous atactic and isotactic block copolymers and their self-assembly into nano- and microscopic vesicles&rdquo;, published in <em>Polym. Chem., </em><em><strong>2021</strong></em><em>, 12, 5377-5389</em>.</p> <p><a href="https://pubs.rsc.org/en/content/articlelanding/2021/PY/D1PY00952D">https://pubs.rsc.org/en/content/articlelanding/2021/PY/D1PY00952D</a></p> <p>Table of contents:</p> <p><strong>1. Figure 1</strong>: Zip archive containing the experimental data (NMR spectra) for the kinetics of the PBO syntheses (<em>Figure 1c</em>) and the PBO-b-PEEGE syntheses (<em>Figure 1d</em>).</p> <p><strong>2. Figure 2</strong>: Zip archive containing the experimental data for <em>Figure 2</em>. Structural characterisation of the (S)-BCP (S)-PBO₂₇-b-(S)-PG₁₄ by ¹H-NMR spectroscopy in methanol-d₄.</p> <p><strong>3. Figure 3</strong>: Zip archive containing the experimental data for <em>Figure 3</em>. Chiral characterisation of the atactic and isotactic BCPs.</p> <p><strong>4. Figure 4</strong>: Zip archive containing the experimental data for <em>Figure 4</em>. TEM and Cryo-TEM characterisation of the SUVs formed by <em>(a)</em> (R/S)-PBO₂₆-b-(R/S)-PG₁₄, <em>(b)</em> (R)-PBO₂₆-b-(R)-PG₁₄ and <em>(c)</em> (S)-PBO₂₇-b-(S)-PG₁₄.</p> <p><strong>5. Figure 5</strong>: Zip archive containing the CLSM images for <em>Figure 5</em>.</p> <p><strong>6. Figure 6</strong>: Zip archive containing the images for <em>Figure 6</em>. Snapshots of the enzyme reaction within the cavity of (R/S)-BCP GUVs <em>(b)</em> with and <em>(c)</em> without reconstituted membrane protein OmpF, recorded by CLSM at different time points</p> <p><strong>7. Figure 7</strong>: Excel file containing the experimental data for <em>Figure 7</em>. Fluorescence intensity development of <em>(a)</em> (R/S)-BCP and <em>(b)</em> PDMS₂₅-b-PMOXA₁₀ GUVs resulting from the reaction of resorufin &beta;-D-galactopyranoside (RGP) with &beta;-galactosidase (&beta;-Gal) to yield fluorescent resorufin.</p> <p><strong>8. Table 1</strong>: Zip archive containing the experimental data for <em>Table 1</em>.</p> <p><strong>9. Table 2</strong>: Zip archive containing the experimental data for <em>Table 2</em>.</p> <p>&nbsp;</p>