MIT

Group by Year

  • 2008
    Hexafluoroisopropanol functionalized polythiophene is able to build up an isotropic self-supporting network structure. The gel network can be melted and then transformed via mech. shearing to form an anisotropic gel with the chains highly aligned along the shearing direction and the conjugated backbones $π$-stacked with respect to each other neighbors. The mechanism by which a dipole functionalized polythiophene can form a reversible network able to be deformed into structurally oriented films may be of interest in the development of novel processing routes for conjugated polymers. [on SciFinder(R)]
  • 2008
    The synthesis and electrochem. properties of novel block copolymers are reported. Three different norbornene derivs. having phenylene-thiophene, phenylene-bithiophene, and phenylene-furan structures were copolymd. with either norbornene or 7-oxanorbornene derivs. via ring-opening metathesis polymn. (ROMP). Block copolymers’ stabilities and solubilities could be improved by hydrogenation of double bonds in the polymer backbone. The block copolymers were subsequently cross-linked by anodic electropolymn. of phenylene-heterocycle moieties, affording conducting polymers. All of these three block copolymers were readily deposited on the electrode substrates, and their cyclic voltammograms (CVs) revealed an excellent reversibility in the redox cycles. [on SciFinder(R)]
  • 2008
    The utility of Sato’s titanium-mediated reduction of alkynes towards the synthesis of all cis-poly(phenylenevinylene)s (PPVs) is demonstrated by the syn-selective reduction of a variety of model diynes as well as a tetrayne. This technique was then applied to the reduction of a poly(phenyleneethynylene) (PPE) to provide the corresponding all-cis PPV polymer.
  • 2008
    The syntheses and spectroscopic properties of eight new push-pull-type near-infrared fluorophores that contain either isobenzofuran or isothianaphthene subunits are presented. The isobenzofuran dyes demonstrate significantly red-shifted absorption compared with their isothianaphthene counterparts, which is attributed to isobenzofuran’s more potent pro-quinoidal character.
  • 2008
    An oligothiophene tweezer molecule, which has two quaterthiophene moieties connected to create an electrochemically activated hinge, has been synthesized. Two-electron oxidation of the tweezer molecule produces an intramolecular pi-dimer between the two oligothiophene moieties at room temperature as confirmed by UV-vis absorption, electrochemistry, and EPR experiments.
  • 2008
    Stable pi-dimers are formed upon oxidation of the model units of proposed calix[4]arene-based molecular actuators in a solvent of low dielectric constant (CH 2Cl 2) at room temperature. Evidence from UV-vis, EPR, and DPV are all in agreement with the pi-dimer formation. In addition, pi-dimer formation is dependent upon the conformational flexibility of the calix[4]arene hinge.
  • 2008
    A new fluorescent turn-on probe (I) for the selective sensing and bioimaging of thiols is reported. In aq. buffer solns. at physiol. pH, thiols cleave the 2,4-dinitrobenzenesulfonyl group to release the red-emissive donor-acceptor fluorophore. The probe displays excellent immunity to interference from nitrogen and oxygen nucleophiles and the imaging of thiols in living cells is demonstrated. [on SciFinder(R)]
  • 2008
    The tensile and compressive properties of triptycene-polycarbonates were tested over 6 orders of magnitude in strain rate. Initially we studied a low mol. wt., low triptycene content PC blended with Iupilon PC and then a series of higher mol. wt., higher triptycene content polymers. The PC blend with only 1.9 wt.% triptycene displayed up to 20% increase in modulus and up to 17% increase in yield strength with elongations over 80% as compared to the Iupilon PC. The higher mol. wt. T-PCs (up to 26 wt.% triptycene) exhibited improvements in modulus by over 20% and improvements in compressive strengths by nearly 50% at both low and high strain rates without any apparent sacrifice to ductility, as compared to Iupilon PC. All samples contg. triptycene units retained transparency and exhibited no signs of crystallinity or phase sepn. Moreover, both the blends and triptycene-PC copolymers displayed significantly altered dynamic mech. spectra, specifically, the emergence of a pronounced, new $\beta$’ relaxation approx. 75° above the traditionally obsd. $\beta$ relaxation in PC (approx. -100°). The enhancement of the mech. properties obsd. provides valuable insights into the unique packing and interactions during plastic flow induced by the presence of triptycene units. [on SciFinder(R)]
  • 2008

    Solid-state chemosensitive organic devices for vapor-phase detection.

    Springer Series in Materials Science
    ,
    vol.
    107
    ,
    p.
    141–184
    ,
    2008
    A review on state-of-the-art vapor-phase solid-state chemosensing org. devices. The individual chem. sensing approaches and their transduction mechanisms are described. [on SciFinder(R)]
  • 2008
    A one-step, one-pot assembly of arylethynylated cyclohexa-meta-phenylenes from meta-dibromide and meta-diboronates was accomplished using a 6-fold Suzuki macrocyclization, without the need for high diln. or slow-addn. techniques. [on SciFinder(R)]
  • 2008
    To date, the cross effect (CE) and thermal mixing (TM) mechanisms have consistently provided the largest enhancements in dynamic nuclear polarization (DNP) experiments performed at high magnetic fields. Both involve a three-spin electron-electron-nucleus process whose efficiency depends primarily on two electron-electron interactions–the interelectron distance R and the correct electron paramagnetic resonance (EPR) frequency separation that matches the nuclear Larmor frequency, /omega(e2)-omega(e1)/ = omega(n). Biradicals, for example, two 2,2,6,6-tetramethyl-piperidine-1-oxyls (TEMPOs) tethered with a molecular linker, can in principle constrain both the distance and relative g-tensor orientation between two unpaired electrons, allowing these two spectral parameters to be optimized for the CE and TM. To verify this hypothesis, we synthesized a series of biradicals–bis-TEMPO tethered by n ethylene glycol units (a.k.a. BTnE)–that show an increasing DNP enhancement with a decreasing tether length. Specifically at 90 K and 5 T, the enhancement grew from approximately 40 observed with 10 mM monomeric TEMPO, where the average R approximately 56 A corresponding to electron-electron dipolar coupling constant omega(d)2 pi = 0.3 MHz, to approximately 175 with 5 mM BT2E (10 mM electrons) which has R approximately 13 A with omega(d)2 pi = 24 MHz. In addition, we compared these DNP enhancements with those from three biradicals having shorter and more rigid tethers-bis-TEMPO tethered by oxalyl amide, bis-TEMPO tethered by the urea structure, and 1-(TEMPO-4-oxyl)-3-(TEMPO-4-amino)-propan-2-ol (TOTAPOL) TOTAPOL is of particular interest since it is soluble in aqueous media and compatible with DNP experiments on biological systems such as membrane and amyloid proteins. The interelectron distances and relative g-tensor orientations of all of these biradicals were characterized with an analysis of their 9 and 140 GHz continuous-wave EPR lineshapes. The results show that the largest DNP enhancements are observed with BT2E and TOTAPOL that have shorter tethers and the two TEMPO moieties are oriented so as to satisfy the matching condition for the CE.
  • 2007
    The incorporation of pendant iptycene units into polyesters creates a novel polymer-chain contour resembling “mol. barbed wire.”. These types of units contain a unique structural property called the internal mol.-free vol. (IMFV) and have been shown to induce steric interactions between polymer chains through the minimization of the IMFV. This process creates a sterically interconnected polymer-chain network with high ductility because of two new mechanisms: mol. threading and mol. interlocking. The ability for these mechanisms to enhance the mech. properties of polyesters is robust across concn. and processing conditions. The size, shape, and concn. of these pendant units affect the mech. behavior, and results indicate that the larger units do not necessarily produce superior tensile properties. However, the mol.-barbed-wire architecture consistently produces enhanced mech. properties compared to the ref. polyester. The particular stress-strain response can be tailored by minute changes to the periphery of the iptycene unit. [on SciFinder(R)]
  • 2007
    Skipping the monomer: A highly efficient reductive aromatization reaction transforms an unconjugated precursor polymer into a high-mol.-wt., butadiyne-linked anthracene homopolymer. Photophys. and electrochem. analyses reveal that some of these new materials display remarkable stability in both neutral and doped states and have unusually low intrinsic band gaps. [on SciFinder(R)]
  • 2007

    Conducting-Polymer-Based Chemical Sensors: Transduction Mechanisms

    Bulletin of the Chemical Society of Japan
    ,
    vol.
    80
    ,
    p.
    2074–2083
    ,
    2007
    A review. Conducting org. polymers, esp., polythiophene and substituted polythiophenes, for use as sensor materials are discussed. The charge transport mechanisms and response toward analytes based on functional groups and charge interactions are outlined. Sensor systems based on triaryl-Me carbocations are described. The design of specific mol. recognition centers to impart selectivity and the nature of the conducting polymer are also discussed. [on SciFinder(R)]
  • 2007
    A review. In this review the authors restrict the discussions to purely fluorescence-based methods using conjugated polymers. Amplification, small ion sensing using amplifying fluorescent conjugated polymers (AFPs), AFPs for detection of explosives, conjugated polyelectrolytes as biosensors, AFPs for detection of small biomols., proteins, and DNA are discussed. [on SciFinder(R)]
  • 2007
    The fluorescence-based detection of nonquenching, multicationic small molecules has been demonstrated using a blue-emitting, polyanionic poly(p-phenylene ethynylene) (PPE) doped with green-emitting exciton traps (anthryl units). Multicationic amines (spermine, spermidine, and neomycin) were found to effectively induce the formation of tightly associated aggregates between the polymer chains in solution. This analyte-induced aggregation, which was accompanied by enhanced exciton migration in the PPE, ultimately led to a visually noticeable blue-to-green fluorescence color change in the solution. The aggregation-based sensor exhibited poor sensitivity toward dicationic and monocationic amines, demonstrating that a conjugated polyelectrolyte sensor relying on nonspecific, electrostatic interactions may still attain a certain level of selectivity.
  • 2007

    Synthesis and mesomorphic properties of rigid-core ionic liquid crystals.

    Journal of the American Chemical Society
    ,
    vol.
    129
    ,
    p.
    14042–52
    ,
    2007
    Ionic liquid crystals combine the unique solvent properties of ionic liquids with self-organization found for liquid crystals. We report a detailed analysis of the structure-property relationship of a series of new imidazolium-based liquid crystals with an extended aromatic core. Investigated parameters include length and nature of the tails, the length of the rigid core, the lateral substitution pattern, and the nature of the counterion. Depending on the molecular structure, two mesophases were observed: a bilayered SmA2 phase and the more common monolayered SmA phase, both strongly interdigitated. Most materials show mesophases stable to high temperatures. For some cases, crystallization could be suppressed, and room-temperature liquid crystalline phases were obtained. The mesomorphic properties of several mixtures of ionic liquid crystals were investigated. Many mixtures showed full miscibility and ideal mixing behavior; however, in some instances we observed, surprisingly, complete demixing of the component SmA phases. The ionic liquid crystals and mixtures presented have potential applications, due to their low melting temperatures, wide temperature ranges, and stability with extra ion-doping.
  • 2007
    Single-walled carbon nanotubes (SWCNTs) and C60 are functionalized by reactions with di-Me acetylenedicarboxylate (DMAD) and alcs. mediated by 4-(dimethylamino)pyridine (DMAP) to give adducts such as the oxocyclopentenofullerene I. The reactions are proposed to occur by addn. of zwitterions generated from DMAP and DMAD to C60 or SWCNTs with concomitant ring closure followed by substitution of the (dimethylamino)pyridinium moiety of the intermediate adducts with alcs. Reaction of SWCNTs with DMAP, DMAD, and 1-dodecanol yields functionalized carbon nanotubes with significantly greater solubilities in org. solvents than unfunctionalized SWCNTs. The structure of I•CS2 is detd. by X-ray crystallog. [on SciFinder(R)]
  • 2007

    A fluorescence turn-on mechanism to detect high explosives RDX and PETN.

    Journal of the American Chemical Society
    ,
    vol.
    129
    ,
    p.
    7254–5
    ,
    2007
    A fluorescent chemosensor to detect satd. nitramine and nitrate ester explosives was devised based on a photochem. redn. reaction. 10-Methyl-9,10-dihydroacridine (AcrH2) was found to transfer a hydride ion equiv. to the high explosives RDX and PETN upon irradn. at 313 nm in degassed acetonitrile solns. Mechanistic photophys. studies indicate that the photoredn. of RDX proceeds via a two-step electron-hydrogen atom transfer reaction, whereas PETN photoredn. proceeds via a three-step electron-proton-electron transfer sequence. A zinc analog was synthesized and found to display an 80- or 25-fold increase in 480 nm emission intensity upon reaction with RDX or PETN, resp. Moreover, the Zn analog was found to be unresponsive to TNT and other common contaminants, in addn. to being photostable under ambient conditions. On the basis of these characteristics, a powerful chemosensor that displays a direct fluorescent response to either RDX or PETN is reported. [on SciFinder(R)]
  • 2007
    Novel fluoride sensory systems were successfully developed. Previously developed method of the fluoride-induced lactonization to fluorescent mols. was detailed, and newly developed fluoride-induced arom. cyclization scheme was introduced. Based on the strategies using the specific affinity of fluoride to silicon, the authors’ systems are highly selective for fluoride ion. Incorporation of the developed sensor to a conjugated polymer has successfully enhanced its sensitivity to fluoride ion. [on SciFinder(R)]