Near-Infrared-Absorbing B-N Lewis Pair-Functionalized Anthracenes: Electronic Structure Tuning, Conformational Isomerism, and Applications in Photothermal Cancer Therapy.

B-N-fused dianthracenylpyrazine derivatives are synthesized to generate new low gap chromophores. Photophysical and electrochemical, crystal packing, and theoretical studies have been performed. Two energetically similar conformers are identified by density functional theory calculations, showing that the core unit adopts a curved saddle-like shape (x-isomer) or a zig-zag conformation (z-isomer). In the solid state, the z-isomer is prevalent according to an X-ray crystal structure of a C6F5-substituted derivative (4-Pf), but variable-temperature nuclear magnetic resonance studies suggest a dynamic behavior in solution. B-N fusion results in a large decrease of the HOMO-LUMO gap and dramatically lowers the LUMO energy compared to the all-carbon analogues. 4-Pf in particular shows significant absorbance at greater than 700 nm while being almost transparent throughout the visible region. After encapsulation in the biodegradable polymer DSPE-mPEG2000, 4-Pf nanoparticles (4-Pf-NPs) exhibit good water solubility, high photostability, and an excellent photothermal conversion efficiency of ∼41.8%. 4-Pf-NPs are evaluated both in vitro and in vivo as photothermal therapeutic agents. These results uncover B-N Lewis pair functionalization of PAHs as a promising strategy toward new NIR-absorbing materials for photothermal applications.

Highly Luminescent Ladderized Fluorene Copolymers Based on B-N Lewis Pair Functionalization.

A new B-N functionalized polyaromatic building block for conjugated hybrid polymers is developed. Bromine-functionalized dipyridylfluorene is first subjected to Lewis-base-directed electrophilic borylation and subsequently incorporated into conjugated polymers via transition-metal-catalyzed cross-coupling reactions. The borane monomer exhibits bright blue luminescence in solution, as a result of the rigid ladder-type structure generated upon electrophilic borylation. Yamamoto coupling gives rise to a homopolymer and Stille coupling to a vinylene-bridged copolymer. Polymerization of the BN-fused ladder molecules leads to large bathochromic shifts in absorption and emission, which are most pronounced for the vinylene-bridged copolymer. The polymers display strong luminescence in solution with quantum yields of 55% and 78% and sub-ns fluorescence lifetimes; the copolymer also exhibits bright yellow luminescence in the solid state when precipitated from solution.

Polysiloxane/Polystyrene Thermo-Responsive and Self-Healing Polymer Network via Lewis Acid-Lewis Base Pair Formation.

The use of thermo-reversible Lewis Pair (LP) interactions in the formation of transient polymer networks is still greatly underexplored. In this work, we describe the synthesis and characterization of polydimethylsiloxane/polystyrene (PDMS/PS) blends that form dynamic Lewis acid-Lewis base adducts resulting in reversible crosslinks. Linear PS containing 10 mol % of di-2-thienylboryl pendant groups randomly distributed was obtained in a two-step one-pot functionalization reaction from silyl-functionalized PS, while ditelechelic PDMS with pyridyl groups at the chain-termini was directly obtained via thiol-ene "click" chemistry from commercially available vinyl-terminated PDMS. The resulting soft gels, formed after mixing solutions containing the PDMS and PS polymers, behave at room temperature as elastomeric solid-like materials with very high viscosity (47,300 Pa·s). We applied rheological measurements to study the thermal and time dependence of the viscoelastic moduli, and also assessed the reprocessability and self-healing behavior of the dry gel.

Thermo-responsive behavior of borinic acid polymers: experimental and molecular dynamics studies.

The thermo-responsive properties of borinic acid polymers were investigated by experimental and molecular dynamics simulation studies. The homopolymer poly(styrylphenyl(tri-iso-propylphenyl)borinic acid) (PBA) exhibits an upper critical solution temperature (UCST) in polar organic solvents that is tunable over a wide temperature range by addition of small amounts of H2O. The UCST of a 1 mg mL(-1) PBA solution in DMSO can be adjusted from 20 to 100 °C by varying the H2O content from ∼0-2.5%, in DMF from 0 to 100 °C (∼3-17% H2O content), and in THF from 0 to 60 °C (∼4-19% H2O). The UCST increases almost linearly from the freezing point of the solvent with higher freezing point to the boiling point of the solvent with the lower boiling point. The mechanistic aspects of this process were investigated by molecular dynamics simulations. The latter indicate rapid and strong hydrogen-bond formation between BOH moieties and H2O molecules, which serve as crosslinkers to form an insoluble network. Our results suggest that borinic acid-containing polymers are promising as new "smart" materials, which display thermo-responsive properties that are tunable over a wide temperature range.

A borinic acid polymer with fluoride ion- and thermo-responsive properties that are tunable over a wide temperature range.

A new type of smart borinic acid polymer with luminescence and multiple stimuli-responsive properties is reported. In DMSO with small amounts of water, the homopolymer PBA shows a tunable upper critical solution temperature (UCST). As the amount of water increases from 0 to 2.5 % (v/v), the UCST rises linearly from 20 °C to 100 °C (boiling point of water). Thus, the thermal responsive behavior can be tuned over a wide temperature range. Furthermore, polymer solutions in DMSO show a reversible response to fluoride ions, which can be correlated to the presence of the Lewis acidic borinic acid groups. Upon addition of fluoride, the polymer becomes soluble because the functional R2BOH groups are converted into ionic [R2BF2](-) groups, but turns insoluble again upon addition of H2O, which reverses this process.

Electron-deficient triarylborane block copolymers: synthesis by controlled free radical polymerization and application in the detection of fluoride ions.

Luminescent triarylborane homo and block copolymers with well-defined chain architectures were synthesized via reversible addition-fragmentation chain transfer polymerization of a vinyl-functionalized borane monomer. The Lewis acid properties of the polymers were exploited in the luminescent detection of fluoride ions. A dual-responsive fluoride sensor was developed by taking advantage of the reversible self-assembly of a PNIPAM-based amphiphilic block copolymer. Anion detection in aqueous solution was realized by introducing positively charged pyridinium moieties along the polymer chain.

Self-assembly of borane end-functionalized polystyrene through tris(1-pyrazolyl)borate (Tp) iron(II) linkages.

Treatment of trimethylsilane-terminated polystyrenes with BBr(3) resulted in the formation of dibromoboryl-functionalized mono- or ditelechelic styrene polymers. Subsequently, the borane moieties were selectively converted to tris(1-pyrazolyl)borate (Tp) moieties capable of transition metal coordination. These novel telechelic polymers assemble into redox-active supramolecular polymer structures upon reaction with Fe(II) as indicated by GPC, UV-vis, and cyclic voltammetry studies.

Weakly coordinating amphiphilic organoborate block copolymers.

Selective functionalization of polystyrene with weakly coordinating organoborate functionalities BAr(4)(-) (Ar = Ph, C(6)F(5)) has been accomplished by a polymer modification strategy. The first examples of perfluoroarylborate block copolymers have been prepared; light scattering and TEM studies confirm the formation of reverse micelles, in which the weakly coordinating anion sites are covered by a shell of "inert" polystyrene. The core of the micelles was successfully loaded with a cationic rhodium complex.

RAFT polymerization of luminescent boron quinolate monomers.

Fluorescent homopolymers and amphiphilic block copolymers were prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization of two new styryl-type organoboron monomers; the fluorescence characteristics of PEO block copolymers in aqueous solution were studied.

A family of main-chain polymeric Lewis acids: synthesis and fluorescent sensing properties of boron-modified polythiophenes.

A new family of main-chain organoborane polymeric Lewis acids (PTh-BAr) that contain Lewis acidic boron groups embedded into a polythiophene backbone has been prepared under mild conditions through tin-boron exchange reaction. When phenyl and pentafluorophenyl groups are attached to boron, blue and green luminescence is observed, respectively, while the attachment of ferrocenyl substituents leads to a characteristic red color. The incorporation of readily accessible highly Lewis acidic groups into the conjugated polymer backbone provides an opportunity for sensing of Lewis basic substrates. For instance, treatment of the polymer containing phenyl substituents on boron with pyridine leads to efficient quenching of the fluorescence, while the polymer containing ferrocenyl groups changes color from dark red to light orange.