Synthesis, Self-assembly, and Crystal Structure of a Shape-Persistent Polyhedral-Oligosilsesquioxane-Nanoparticle-Tethered Perylene Diimide

Abstract

A novel organic-inorganic hybrid with two polyhedral oligosilsesquioxane (POSS) nanoparticles covalently attached to perylene diimide (PDI) via a rigid 1,4-phenylene linkage (POSS-PDI-POSS) was designed and synthesized to examine the effect of bulky and well-defined nanoparticle side chains on the self-assembly behavior of PDI derivatives. The molecules were self-assembled directly by slow evaporation of a cast drop from solution in tetrahydrofuran to give rise to uniform crystalline nanobelts with dimensions typically of 0.2 mm × 1 µm × 50 nm. The phase behavior and crystal structure of the sample were then elucidated via a combination of different experimental techniques such as differential scanning calorimetry (DSC), wideangle X-ray diffraction (WAXD), selected area electron diffraction (SAED) in transmission electron microscopy (TEM), polarized light microscopy, and atomic force microscopy. One-dimensional (1D) WAXD and DSC revealed that only one crystalline phase exists. Based on the 2D WAXD fiber pattern obtained from the oriented POSS-PDI-POSS samples, the crystalline structure was determined to be a triclinic unit cell with dimensions of a ) 6.577 nm, b ) 5.213 nm, c ) 1.107 nm, R ) 93.26°, β ) 94.85°, and γ ) 92.73°, which was confirmed by SAED experiments on the single crystals with different crystal zone orientations. The detailed molecular conformational analysis indicated that the steric hindrance of the POSS nanoparticles covalently attached to PDI via a rigid 1,4-phenylene linkage makes it difficult to achieve a continuous stacking of PDIs. Instead, the molecules dimerized to maximize the π-π interaction. The dimers then became the building blocks and packed themselves into the unit cell. This strong tendency for dimerization was supported by concentration-dependent ultraviolet/visible absorption spectra, florescence spectra, and tandem mass spectroscopy with traveling wave ion mobility separation. The combined SAED and TEM results showed that the c*-axis of the crystal is along the elongated direction of the single-crystal nanobelt and the normal direction of the π-π stacking is along the a*-axis. A crystal structure with six dimers as one supramolecular motif in one unit cell was proposed to account for the unusually large unit cell dimensions. The complex structure could be attributed to the longitudinal, transverse, and slightly rotational offsets between the PDIs in the dimers and interdigitated neighboring dimers due probably to both electrostatic interactions and steric demands. The molecular packing scheme in the crystal was simulated using Cerius 2 software, and the resulting diffraction data agreed well with the experimental results. The rationale for such 1D nanostructured morphology formation is also discussed.

Reactive bay functionalized perylene monoimide-polyhedral oligomeric silsesquioxane organic electronic dye

“…We have previously crystallized POSS-PDI-POSS and formed one dimensional crystals, which were triclinic in nature [35]. Similar results have been obtained when we crystallized POSS-PDI Br -POSS.…”

“…Taking advantage of the bulkiness of POSS to suppress the π-π interaction in PDI, we have previously end-capped planar PDI with POSS and reported on its photophysical properties [35]. Similar molecular structure has been investigated by other groups [36,37].…”

“…The use of POSS on the N-imide has been reported to change only slightly the characteristic solution UV-Vis absorption and photoluminescence properties of PDI [34,35]. Monoimidizing PDI with POSS and bay functionalizing it with bromine to form POSS-PDI Br is expected to alter the POSS-PDI Br -POSS solid state absorption and luminescent properties.…”

Regioisomeric Tandem Triblock Shape Amphiphiles Based on Polyhedral Oligomeric Silsesquioxanes

“…Previous examples consistm ostly of "diblocks" and there are only limited examples of "triblocks" (like the cube-plane-cube conjugates,P OSS-PDI-POSS). [12] Similar to the scenario in multiblock copolymers, [13] tandem, multiblock shape amphiphiles are attractive candidates for generating complex structures. For example, the AB n dendron-like shape amphiphiles exhibit versatile phase structures, including those unconventional phases in soft matter such as Frank-Kasper A15 and sigma phases.…”

Mehrdimensionale Massenspektrometrie von synthetischen Polymeren und modernen Materialien

“…Laut Molekülmodellierung sollte eine optimale π‐π‐Überlappung durch schräg oder längs versetzte PDI‐Ebenen (wie bei B bzw. C) erreicht wird . Die Längsversetzung ermöglicht auch eine weitere Stabilisierung durch Wasserstoffbrückenbindungen zwischen den Hydroxy‐Endgruppen und den Carbonylgruppen von PDI (D), während eine Wasserstoffbrückenbindung zwischen den Hydroxy‐Endgruppen (A) die Stabilität des Dimers aufgrund der ineffektiven π‐π‐Überlappung erheblich verringert.…”