Direct patterning of composite biocompatible microstructures using microfluidics

This study demonstrates a versatile and fast method for patterning three-dimensional (3D) monolithic microstructures made of multiple (up to 24 demonstrated) types of materials, all spatially aligned, inside a microchannel. This technique uses confocal scanning or conventional fluorescence microscopy to polymerize selected regions of a photocurable material, and microfluidics to automate the delivery of a series of washes and photocurable reagents. Upon completion of lithographic cycles, the aligned 3D microstructures are suitable for microfluidic manipulation and analysis. We demonstrated the fabrication of composite 3D microstructures with various geometries, size scales (up to 1 mm2), spatial resolution (down to 3 microm), and materials. For a typical multi-cycle process, the total fabrication time was tens of minutes, compared to tens of hours for conventional methods. In the case of 3D hydrogels, a potential use is the direct patterning of inhomogeneous 3D microenvironments for studying cell behavior.     

X-ray-excited optical luminescence (XEOL) and X-ray absorption fine structures (XAFS) studies of gold(I) complexes with diphosphine and bipyridine ligands

Synchrotron techniques, X-ray-excited optical luminescence (XEOL) combined with X-ray absorption fine structures (XAFS), have been used to study the electronic structure and optical properties of a series of luminescent gold(I) complexes with diphosphine and bipyridine ligands using tunable X-rays (in the regions of the C and P K-edges and the Au L3-edge) and UV from synchrotron light sources. The effects of gold-ligand and aurophilic interactions on the luminescence from these gold(I) complexes have been investigated. It is found that the luminescence from these complexes is phosphorescence, primarily due to the decay of the Au (5d) --> PR3 (pi*), metal to ligand charge transfer (MLCT) excitation as well as contributions from the conjugated pi-system in the bipyridine ligands via the gold-nitrogen bond. The large Au 5d spin-orbit coupling enhances the intersystem crossing. The elongation of the hydrocarbon chain of the diphosphine ligand does not greatly affect the spectral features of the luminescence from the gold(I) complexes. However, the intensity of the luminescence was reduced significantly when the bipyridine ligand was replaced with 1,2-bis(4-pyridylamido)benzene. The aurophilic interaction, as investigated by EXAFS at the Au L3-edge, is shown to be only one of the factors that contribute to the luminescence of the complexes.     

Regioselective Formation of Enediynes via Intramolecular Trapping of Allylic Cations

Enediynes are a novel class of naturally occurring antitumor antibiotics capable of causing DNA strand cleavage by hydrogen atom abstraction from the deoxyribose backbone. During the past decade, numerous synthetic methods have been developed to synthesize the naturally occurring and the "designed" enediynes for biomedical studies. Recently, we have succeeded in assembling the cis-enediynes 2 by a novel and high-yielding allylic rearrangement under mild reaction conditions (Eq 1).^1-3 This methodology has been used to synthesize a 10-membered ring enediyne³ which exhibits DNA cleavage activity.     

Temperature‐induced phase transition of poly(N‐n‐propylacrylamide‐co‐butyl methacrylate‐co‐N,N‐diethylaminoethyl methacrylate)

Terpolymers composed of N‐n‐propylacrylamide (NPAAm), butyl methacrylate (BMA), and N,N‐diethylaminoethyl methacrylate (DEAEMA) were prepared in an attempt to investigate the temperature‐induced phase transition and its mechanism. Poly(NPAAm) showed the lower critical solution temperature (LCST) around 24°C in water. With the incorporation of DEAEMA with NPAAm, the LCST change was characterized by an initial increase. However, the LCST was shifted to the lower temperature at the later stage. This might be explained in terms of hydrophilic/hydrophobic contribution of DEAEMA to the LCST. The swelling behavior of copolymer gel in the various solvents and spin‐lattice relaxation time (T₁) study by NMR strongly suggested the hydrophilic/hydrophobic contribution of DEAEMA to the LCST depending on the local environment. © 1999 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 37: 1407–1411, 1999     

Tough and tunable adhesion of hydrogels: experiments and models

As polymer networks infiltrated with water, hydro-gels are major constituents of animal and plant bodies and have diverse engineering applications. While natural hydro-gels can robustly adhere to other biological materials, such as bonding of tendons and cartilage on bones and adhe-sive plaques of mussels, it is challenging to achieve such tough adhesions between synthetic hydrogels and engineer-ing materials. Recent experiments show that chemically anchoring long-chain polymer networks of tough synthetic hydrogels on solid surfaces create adhesions tougher than their natural counterparts, but the underlying mechanism has not been well understood. It is also challenging to tune sys-tematically the adhesion of hydrogels on solids. Here, we provide a quantitative understanding of the mechanism for tough adhesions of hydrogels on solid materials via a com-bination of experiments, theory, and numerical simulations. Using a coupled cohesive-zone and Mullins-effect model val-idated by experiments, we reveal the interplays of intrinsic work of adhesion, interfacial strength, and energy dissipation in bulk hydrogels in order to achieve tough adhesions. We fur-ther show that hydrogel adhesion can be systematically tuned by tailoring the hydrogel geometry and silanization time of solid substrates, corresponding to the control of energy dis-sipation zone and intrinsic work of adhesion, respectively. The current work further provides a theoretical foundation for rational design of future biocompatible and underwater adhesives.     

Strong optical field study of a single self-assembled quantum dot

We review the investigation of a single quantum dot driven by a strong optical field. By coherent pump-probe spectroscopy, we demonstrate the Autler–Townes splitting and Mollow absorption spectrum in a single neutral quantum dot. Furthermore, we also show the typical Mollow absorption spectrum by driving a singly charged quantum dot in a strong optical coupling regime. Our results show all the typical features of an isolated atomic system driven by a strong optical field, such as the AC stark effect, Rabi side bands and optical gain effect, which indicate that both neutral and charged quantum dots maintain the discrete energy level states even at high optical field strengths.     

Reduction of Disilane (tBu3Si)Br2Si‐SiBr2(SitBu3) in Presence of C2H4: A Mechanistic Approach

The reduction of R*–SiBr₂–SiBr₂–R* ( 2 ) with NaR* (R* = supersilyl = SitBu₃) in presence of C₂H₄ provides a white crystalline solid (η²‐C₂H₄)R*Si–SiR*(Br)(CH₂–CH₂–R*) ( 3 ) characterized by X‐ray diffraction analysis. Compound 3 is accompanied with an impurity of R*(Br)₂Si–Si(Br)(R*)(CH₂–CH₂–R*) ( 4 ). The formation of 3 and 4 runs complicated because of several reactive partners. However, reduction of 2 with sodium naphthalenide in presence of ethene runs straightforward with formation of a mixture of tetrahedrane R*₄Si₄ ( 1 ) and bis(silirane) R*(η²‐C₂H₄)Si–Si(η²‐C₂H₄)R* ( 5 ). The latter is formed by [1+2]‐cycloaddition reaction of intermediate disilyne R*Si≡SiR* with ethene. Compound 5 has been characterized by X‐ray structure determination. The ¹H NMR spectrum of the silacyclopropane ring protons shows AA′BB′ complex spectrum comprising of 2 sets each of 12 transitions.