MIT

Group by Year

  • 2013
    New tetraalkylcyclobutadiene-C60 adducts are developed via Diels-Alder cycloaddn. of C60 with in situ generated cyclobutadienes. The cofacial $π$-orbital interactions between the fullerene orbitals and the cyclobutene are shown to decrease the electron affinity and thereby increase the LUMO (LUMO) energy level of C60 significantly (ca. 100 and 300 meV for mono- and bisadducts, resp.). These variations in LUMO levels of fullerene can be used to generate higher open-circuit voltages (VOC) in bulk heterojunction polymer solar cells. The tetramethylcyclobutadiene-C60 monoadduct displays an open-circuit voltage (0.61 V) and a power conversion efficiency (2.49%) comparable to the widely used P3HT/PCBM (poly(3-hexylthiophene/([6,6]-phenyl-C61-butyric acid Me ester) composite (0.58 V and 2.57%, resp.). The role of the cofacial $π$-orbital interactions between C60 and the attached cyclobutene group was probed chem. by epoxidn. of the cyclobutene moiety and theor. through d. functional theory calcns. The electrochem., photophys., and thermal properties of the newly synthesized fullerene derivs. support the proposed effect of functionalization on electron affinities and photovoltaic performance. [on SciFinder(R)]
  • 2013
    Three different types of epoxy-functionalized multi-walled carbon nanotubes (EpCNTs) were prepd. by multiple covalent functionalization methods. The EpCNTs were characterized by thermogravimetric anal. (TGA), IR spectroscopy (FTIR), and Raman spectroscopy to confirm covalent functionalization. The effect of the different chemistries on the adhesive properties was compared to a neat com. epoxy (Hexion formulation 4007) using functionalized and unfunctionalized multi-walled carbon nanotubes (MWCNT) at 0.5, 1, 2, 3, 5, and 10 wt%. It was found that an EpCNT at 1 wt% increased the lap shear strength, tested using the American Society for Testing and Materials std. test D1002, by 36% over the unfilled epoxy formulation and by 27% over a 1 wt% unmodified MWCNT control sample. SEM images revealed a fracture surface morphol. change with the incorporation of EpCNT and a deflection of the crack fronts at the site of embedded CNTs, as the mechanism accounting for increased adhesive strength. Rheol. studies showed non-linear viscosity and DSC cure studies showed an alteration of cure kinetics with increased CNT concn., and these effects were more pronounced for EpCNT. [on SciFinder(R)]
  • 2013
    Several new triptycene-containing polyetherolefins were synthesized via acyclic diene metathesis (ADMET) polymerization. The well-established mechanism, high selectivity and specificity, mild reaction conditions, and well-defined end-groups make the ADMET polymerization a good choice for studying systematic variations in polymer structure. Two types of triptycene-based monomer with varying connectivities were used in the synthesis of homopolymers, block copolymers, and random copolymers. In this way, the influence of the triptycene architecture and concentration in the polymer backbone on the thermal behavior of the polymers was studied. Inclusion of increasing amounts of triptycene were found to increase the glass transition temperature, from 44 degrees C in polyoctenamer to 59 degrees C in one of the hydrogenated triptycene homopolymers (H-PT2). Varying the amounts and orientations of triptycene was found to increase the stiffness (H-PT1), toughness (PT11-b-PO1) and ductility (PT11-ran-PO3) of the polymer at room temperature. (c) 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013, 51, 1695-1706
  • 2013
    Several solvent-free processing methods to disperse multiwalled carbon nanotubes (MWCNTs) in bisphenol F-based epoxy resin were investigated, including the use of a microfluidizer (MF), planetary shear mixer (PSM), ultrasonication (US) and combinations. The processed mixture was cured with diethyl toluene diamine. Three complimentary techniques were used to characterize the dispersion of the MWCNTs in cured composite samples: optical microscopy, micro Raman spectroscopy, and scanning electron microscopy (SEM). For sample MF + PSM, optical micrographs and Raman images showed reduced agglomeration and a homogeneous distribution of MWCNTs in the epoxy matrix. SEM analysis of fractured specimen after tensile testing revealed breakage of nanotubes along the fracture surface of the composite. A comparison of the MWCNT dispersion in the epoxy samples processed using different methods showed that a combination of MF and PSM processing yields a more homogeneous sample than the PSM or US + PSM processed samples. Mechanical testing of the composites showed about 15% improvement in the tensile strength of samples processed by the MF + PSM method over other methods. Thermogravimetric analysis (TGA) results showed a small decrease in the onset degradation temperature for poorly dispersed samples produced by PSM compared with the well-mixed samples (MF + PSM). These results strongly suggest that the MF + PSM processing method yield better-dispersed and stronger MWCNT/epoxy composites. (c) 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2013
  • 2013
    Photoalignment of nematic liquid crystals is demonstrated using a di-$π$-methane rearrangement of a designed polymer. The alignment mechanism makes use of the strong coupling of the liquid crystal directors to dibenzobarrelene groups. The large structural changes that accompany photoisomerization effectively passivate segments of the polymer, allowing the remaining dibenzobarrelene groups to dominate the director alignment. Photoisomerization requires triplet sensitization, and the polymer was designed to have a uniaxially fixed rigid structure and rapid triplet energy transfer from the proximate benzophenone units to the dibenzobarrelene groups. The isomerization was observed to be regiospecific, and thin films showed alignment.
  • 2013
    We report direct (13)C dynamic nuclear polarization at 5 T under magic-angle spinning (MAS) at 82 K using a mixture of monoradicals with narrow EPR linewidths. We show the importance of optimizing both EPR linewidth and electron relaxation times by studying direct DNP of (13)C using SA-BDPA and trityl radical, and achieve (13)C enhancements above 600. This new approach may be best suited for dissolution DNP and for studies of (1)H depleted biological and other nonprotonated solids.
  • 2013
    Dynamic nuclear polarization (DNP) of amorphous and crystalline ortho-terphenyl (OTP) in the absence of glass forming agents is presented in order to gauge the feasibility of applying DNP to pharmaceutical solid-state nuclear magnetic resonance experiments and to study the effect of intermolecular structure, or lack thereof, on the DNP enhancement. By way of (1)H-(13)C cross-polarization, we obtained a DNP enhancement ($ε$) of 58 for 95% deuterated OTP in the amorphous state using the biradical bis-TEMPO terephthalate (bTtereph) and $ε$ of 36 in the crystalline state. Measurements of the (1)H T1 and electron paramagnetic resonance experiments showed the crystallization process led to phase separation of the polarization agent, creating an inhomogeneous distribution of radicals within the sample. Consequently, the effective radical concentration was decreased in the bulk OTP phase, and long-range (1)H-(1)H spin diffusion was the main polarization propagation mechanism. Preliminary DNP experiments with the glass-forming anti-inflammation drug, indomethacin, showed promising results, and further studies are underway to prepare DNP samples using pharmaceutical techniques.
  • 2013

    Rapid prototyping of carbon-based chemiresistive gas sensors on paper.

    Proceedings of the National Academy of Sciences of the United States of America
    ,
    vol.
    110
    ,
    p.
    E3265–E3270,SE3265/1–SE3265/28
    ,
    2013
    Chem. functionalized carbon nanotubes (CNTs) are promising materials for sensing of gases and volatile org. compds. However, the poor soly. of carbon nanotubes hinders their chem. functionalization and the subsequent integration of these materials into devices. This manuscript describes a solvent-free procedure for rapid prototyping of selective chemiresistors from CNTs and graphite on the surface of paper. This procedure enables fabrication of functional gas sensors from com. available starting materials in <15 min. The 1st step of this procedure involves the generation of solid composites of CNTs or graphite with small mol. selectors-designed to interact with specific classes of gaseous analytes-by solvent-free mech. mixing in a ball mill and subsequent compression. The 2nd step involves deposition of chemiresistive sensors by mech. abrasion of these solid composites onto the surface of paper. Parallel fabrication of multiple chemiresistors from diverse composites rapidly generates cross-reactive arrays capable of sensing and differentiating gases and volatile org. compds. at part-per-million and part-per-thousand concns. [on SciFinder(R)]
  • 2013
    The synthesis of a long-lived, truxene-based radical that is highly delocalized and exhibits a narrow EPR absorption is reported. The radical is stable for multiple hours in a soln. exposed to air and remains for months in the solid state under inert gas. Characterization and properties are discussed. [on SciFinder(R)]
  • 2013

    We have developed highly fluorescent multiblock conjugated polymer nanoparticles for bioimaging and in vivo tumor targeting. We have shown that folate functionalized conjugated polymer nanoparticles exhibit preferential cell assocn. and uptake in vitro compared to non-functionalized nanoparticles. [on SciFinder(R)]

  • 2013
    An octabenzo [12]cycloparaphenylene I (nanohoop) was prepd. in four steps as a potential precursor to a perylene-like cycloparaphenylene. Addn. of the lithium reagent derived from 1,4-dibromonaphthalene to 1,4-cyclohexanedione, O-methoxymethylation and isolation of the cis-dinaphthylcyclohexane, nickel-catalyzed macrocyclization, and acid- and microwave-mediated aromatization yielded I in 0.34% overall yield. The absorption and emission spectra of I and of its unaromatized precursor were obtained and compared. [on SciFinder(R)]
  • 2013
    The accessible concn. of exfoliated and undamaged multi-walled carbon nanotubes (MWCNTs) in polymer nanocomposites is an essential issue to the future of these materials. In this work, we report two methodologies directed at obtaining elec. conducting poly(styrene-b-(ethylene-co-butylene)-b-styrene) (SEBS) nanocomposites with different MWCNT contents. The first depends on the time modulation of ultrasonication of toluene mixts., whereas the second relies on the use of alkyl-functionalized MWCNTs (f-MWCNTs). UV-vis spectroscopy investigations and thermogravimetric analyses allowed the quantification of exfoliated CNTs incorporated in the SEBS mixt. TEM micrographs denoted that a prolonged sonication time (40 min) induced an extensive MWCNTs degrdn. (av. length decreased of 40%), which affected the elec. cond. of the nanocomposites. The f-MWCNTs appeared to be more effective in prepg. SEBS nanocomposites due to the higher dispersion efficiency, negligible nanotube degrdn. and higher elec. cond.The temp. dependence of the resistance of the SEBS/MWCNT system was investigated in the range 20-60 °C to explore its potential for sensor development. [on SciFinder(R)]
  • 2013
    Interfacial/in situ oxidative polymn. of polypyrrole in the presence of functionalized graphene sheets produces high-quality composites for supercapacitors, as analyzed by electrochem. impedance spectroscopy and cyclic voltammetry anal. The synergistic interaction induced by the growth of p-type polypyrrole on the surface of neg. charged carboxylate functionalized graphene sheets results in higher storage capacity than graphene-only or polymer-only films. The high cond. of p-doped polypyrrole and high surface area of graphene promote high charge accumulation in capacitors. The authors report the optimization of the relative concns. of carboxylate functionalized graphene in the polypyrrole matrix to maximize the compn.’s capacitance to 277.8 F/g. [on SciFinder(R)]
  • 2013
    The authors describe the first study of trinuclear gold(I) pyrazolates on the mol. level by time-dependent scanning tunneling microscopy (STM). On the graphite/1-octanoic acid interface, dodecyl-functionalized gold pyrazolates formed concn.-controlled morphologies. The authors found two types of monomeric packing and one dimeric type with two trinuclear gold pyrazolates next to each other on the surface. For an octadecyl-functionalized deriv., all studied concns. resulted in a dimeric morphol. However, different concns. led to different transient states during the layer evolution. At low concns., a transient monomeric state was present with the alkyl chains in a gauche-conformation that subsequently converted to a more optimized anti-conformation. At higher concns. a less stable “line” polymorph was obsd. The confinement of the mols. to the surface led to cooperative dynamics, in which two mols. in a dimer moved as if they were one particle. Furthermore, in a higher level of cooperativity, the rotation of one dimer appears to induce rotations in coupled neighboring dimers. [on SciFinder(R)]
  • 2013

    Robust Cyclohexanone Selective Chemiresistors Based on Single-Walled Carbon Nanotubes.

    Analytical Chemistry (Washington, DC, United States)
    ,
    vol.
    85
    ,
    p.
    7154–7158
    ,
    2013
    Functionalized single-walled carbon nanotube (SWCNT)-based chemiresistors are reported for a highly robust and sensitive gas sensor to selectively detect cyclohexanone, a target analyte for explosive detection. The trifunctional selector has three important properties: it noncovalently functionalizes SWCNTs with cofacial $π$-$π$ interactions, it binds to cyclohexanone via hydrogen bond (mechanistic studies were studied), and it improves the overall robustness of SWCNT-based chemiresistors (e.g., humidity and heat). The authors’ sensors produced reversible and reproducible responses in <30 s to 10 ppm of cyclohexanone and displayed an av. theor. limit of detection (LOD) of 5 ppm. [on SciFinder(R)]
  • 2013
  • 2013
    PURPOSE: The goal was to identify molecular imaging probes that would enter the brain, selectively bind to Parkinson’s disease (PD) pathology, and be detectable with one or more imaging modalities. PROCEDURE: A library of organic compounds was screened for the ability to bind hallmark pathology in human Parkinson’s and Alzheimer’s disease tissue, alpha-synuclein oligomers and inclusions in two cell culture models, and alpha-synuclein aggregates in cortical neurons of a transgenic mouse model. Finally, compounds were tested for blood-brain barrier permeability using intravital microscopy. RESULTS: Several lead compounds were identified that bound the human PD pathology, and some showed selectivity over Alzheimer’s pathology. The cell culture models and transgenic mouse models that exhibit alpha-synuclein aggregation did not prove predictive for ligand binding. The compounds had favorable physicochemical properties, and several were brain permeable. CONCLUSIONS: Future experiments will focus on more extensive evaluation of the lead compounds as PET ligands for clinical imaging of PD pathology.[on SciFinder (R)]
  • 2013
    During the three decades 1980-2010, magic angle spinning (MAS) NMR developed into the method of choice to examine many chemical, physical, and biological problems. In particular, a variety of dipolar recoupling methods to measure distances and torsion angles can now constrain molecular structures to high resolution. However, applications are often limited by the low sensitivity of the experiments, due in large part to the necessity of observing spectra of low-$\gamma$ nuclei such as the I = 1/2 species (13)C or (15)N. The difficulty is still greater when quadrupolar nuclei, such as (17)O or (27)Al, are involved. This problem has stimulated efforts to increase the sensitivity of MAS experiments. A particularly powerful approach is dynamic nuclear polarization (DNP) which takes advantage of the higher equilibrium polarization of electrons (which conventionally manifests in the great sensitivity advantage of EPR over NMR). In DNP, the sample is doped with a stable paramagnetic polarizing agent and irradiated with microwaves to transfer the high polarization in the electron spin reservoir to the nuclei of interest. The idea was first explored by Overhauser and Slichter in 1953. However, these experiments were carried out on static samples, at magnetic fields that are low by current standards. To be implemented in contemporary MAS NMR experiments, DNP requires microwave sources operating in the subterahertz regime, roughly 150-660 GHz, and cryogenic MAS probes. In addition, improvements were required in the polarizing agents, because the high concentrations of conventional radicals that are required to produce significant enhancements compromise spectral resolution. In the last two decades, scientific and technical advances have addressed these problems and brought DNP to the point where it is achieving wide applicability. These advances include the development of high frequency gyrotron microwave sources operating in the subterahertz frequency range. In addition, low temperature MAS probes were developed that permit in situ microwave irradiation of the samples. And, finally, biradical polarizing agents were developed that increased the efficiency of DNP experiments by factors of ∼4 at considerably lower paramagnet concentrations. Collectively, these developments have made it possible to apply DNP on a routine basis to a number of different scientific endeavors, most prominently in the biological and material sciences. This Account reviews these developments, including the primary mechanisms used to transfer polarization in high frequency DNP, and the current choice of microwave sources and biradical polarizing agents. In addition, we illustrate the utility of the technique with a description of applications to membrane and amyloid proteins that emphasizes the unique structural information that is available in these two cases.
  • 2013

    Conjugated Amplifying Polymers for Optical Sensing Applications.

    ACS Applied Materials & Interfaces
    ,
    vol.
    5
    ,
    p.
    4488–4502
    ,
    2013
    A review. Thanks to their unique optical and electrochem. properties, conjugated polymers have attracted considerable attention over the last 2 decades and resulted in numerous technol. innovations. In particular, their implementation in sensing schemes and devices was widely studied and produced a multitude of sensory systems and transduction mechanisms. Conjugated polymers possess numerous attractive features that make them particularly suitable for a broad variety of sensing tasks. They display sensory signal amplification (compared to their small-mol. counterparts) and their structures can easily be tailored to adjust soly., absorption/emission wavelengths, energy offsets for excited state electron transfer, and/or for use in soln. or in the solid state. This versatility has made conjugated polymers a fluorescence sensory platform of choice in the recent years. In this review, the authors highlight a variety of conjugated polymer-based sensory mechanisms together with selected examples from the recent literature. [on SciFinder(R)]
  • 2013
    We report the concise synthesis of a symmetrical monomer that provides a head-to-head pyridine building block for the preparation of cationic conjugated polymers. The obtained poly(pyridinium-phenylene) polymers display appealing properties such as high electron affinity, charge-transport upon n-doping, and optical response to electron-donating analytes. A simple assay for the optical detection of low micromolar amounts of a variety of analytes in aqueous solution was developed. In particular, caffeine could be measured at a 25 $μ$M detection limit. The reported polymers are also suitable for layer-by-layer film formation.