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61.
Santosh Kumar Sejy Lee Reju George Thomas Seung‐Jea Lee Hong‐Joon Lee In‐Kyu Park Yong Yeon Jeong Tae‐Ho Yoon Dong‐Chan Shin Jae‐Suk Lee 《Journal of polymer science. Part A, Polymer chemistry》2019,57(11):1165-1172
Self‐emulsion polymerization (SEP), a green route developed by us for the polymerization of amphiphilic monomers, does not require any emulsifier or an organic solvent except that the water‐soluble initiators such as 2,2′‐azobis[2‐(2‐imidazolin‐2‐yl)propane]dihydrochloride (VA‐044) and potassium persulfate (KPS) are only used. We report here the polymer nanoscaffolds from a number of amphiphilic monomers, which can be used for in situ encapsulation of a variety of nanoparticles. As a demonstration of the efficacy of these nanoscaffolds, the synthesis of a biocompatible hybrid nanoparticle (nanohybrid), prepared by encapsulating Fe3O4 magnetic nanoparticle (Fe3O4 MNPs) in poly(2‐hydroxyethyl methacrylate) in water, for MRI application is presented. The nanohybrid prepared following the SEP in the form of an emulsion does not involve the use of any stabilizing agent, crosslinker, polymeric emulsifier, or surfactant. This water‐soluble, spherical, and stable nanohybrid containing Fe3O4 MNPs of average size 10 ± 2 nm has a zeta potential value of ?41.89 mV under physiological conditions. Magnetic measurement confirmed that the nanohybrid shows typical magnetic behavior having a saturation magnetization (Ms) value of 32.3 emu/g and a transverse relaxivity (r2) value of 29.97 mM?1 s?1, which signifies that it can be used as a T2 contrast agent in MRI. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 相似文献
62.
Yu Na Lim Soo Kyung Chae Woongbin Yim Ji‐Yong Park Woojin Yoon Hoseop Yun Eunha Kim Seung Uk Son Hye‐Young Jang 《应用有机金属化学》2019,33(3)
The reaction of [(domppp) Pd (OAc)2] [domppp = 1,3‐bis (di‐o‐methoxyphenylphosphino)propane] and imidazolium‐functionalized carboxylic acids containing various anions (Br?, PF6?, SbF6? and BF4?) resulted in the formation of nano‐sized Pd (II) aggregates under template‐free conditions. The rate of formation of aggregates can be modulated by changing the anion, affecting the rate of polymerization of CO and olefins without fouling. Herein, we describe the analysis of Pd (II) catalysts by dynamic light scattering, atomic force microscopy, X‐ray photoelectron spectroscopy and X‐ray crystallography, and co‐ and terpolymerization results including the catalytic activity, and bulk density and molecular weight of polymers. 相似文献
63.
64.
Choi SJ Yoo PJ Baek SJ Kim TW Lee HH 《Journal of the American Chemical Society》2004,126(25):7744-7745
We describe a novel UV-curable mold that is stiff enough for replicating dense sub-100-nm features even with a high aspect ratio. It also allows for flexibility when the mold is prepared on a flexible support such that large area replication can be accomplished. The composite material of the mold is inert to chemicals and solvents. The surface energy is made low with a small amount of releasing agent such that the mold can be removed easily and cleanly after patterning. In addition, the material allows self-replication of the mold. These unique features of the mold material should make the mold quite useful for various patterning purposes. 相似文献
65.
The preparation of an 1,3-alternate calix[4]arene phosphorus ligand, 25,27-bis(2-(diphenylphosphino)ethoxy)-26,28-bis(1-propyloxy)calix[4]arene (3), is presented. Ligand 3 is obtained in three steps in 64% overall yield. Reaction of 3 with [Rh(cot)2]BF4 produced the encapsulated rhodium complex [Rh[(P,P)-diphen-calix[4]arene]]BF4 (4). As revealed by a single-crystal X-ray diffraction study, the rhodium center has a bent coordination environment with a P-Rh-P angle of 135.66(3) degrees. Palladation of 3 employing [Pd(MeCN)4](BF4)2 yielded the chelate palladium complex 7 in which the palladium center has a slightly bent configuration. Treatment of the ligand with Pd(cod)Cl2 and [Pd(eta3-C4H7)(THF)2]BF4 leads to the isolation of the monometallic complex. Full characterization includes X-ray structural studies of compounds 3, 4, and 6. 相似文献
66.
Mohd Yusuf Khan Xiangxiong Chen Seung Woo Lee Seok Kyun Noh 《Macromolecular rapid communications》2013,34(15):1225-1230
Atom transfer radical polymerization (ATRP) catalyzed by high oxidation state metal salts of FeX3 is developed for the first time in the absence of both external initiator and reducing agent. Methyl methacrylate (MMA) and styrene are polymerized successfully using FeX3/Phosphorous ligands with well‐controlled molecular weight distributions (=1.5). The molecular weight of the polymers increases with monomer consumption with the progress of time and the polymerization behaviors show a decent ATRP trend. Activators and initiators are suggested to generate in situ by the addition reaction of MMA and one equivalent of FeX3. The PMMA synthesized from without‐initiator system is characterized by 1H, 13C and DEPT (distortionless enhancement by polarization transfer nuclear magnetic resonance) nuclear magnetic resonance spectroscopy. Chain extension and copolymerization experiments prove the livingness of the obtained polymer.
67.
Kim MS Sim TS Kim YJ Kim SS Jeong H Park JM Moon HS Kim SI Gurel O Lee SS Lee JG Park JC 《Lab on a chip》2012,12(16):2874-2880
Circulating tumor cells (CTCs) have gained increasing attention as physicians and scientists learn more about the role these extraordinarily rare cells play in metastatic cancer. In developing CTC technology, the critical criteria are high recovery rates and high purity. Current isolation methods suffer from an inherent trade-off between these two goals. Moreover, ensuring minimal cell stress and robust reproducibility is also important for the clinical application of CTCs. In this paper, we introduce a novel CTC isolation technology using selective size amplification (SSA) for target cells and a multi-obstacle architecture (MOA) filter to overcome this trade-off, improving both recovery rate and purity. We also demonstrate SSA-MOA's advantages in minimizing cell deformation during filter transit, resulting in more stable and robust CTC isolation. In this technique, polymer microbeads conjugated with anti-epithelial cell adhesion molecules (anti-EpCAM) were used to selectively size-amplify MCF-7 breast cancer cells, definitively differentiating from the white blood cells (WBCs) by avoiding the size overlap that compromises other size selection methods. 3 μm was determined to be the optimal microbead diameter, not only for size discrimination but also in maximizing CTC surface coverage. A multi-obstacle architecture filter was fabricated using silicon-on-glass (SOG) technology-a first such application of this fabrication technique-to create a precise microfilter structure with a high aspect ratio. The filter was designed to minimize cell deformation as simulation results predicted that cells captured via this MOA filter would experience 22% less moving force than with a single-obstacle architecture. This was verified by experiments, as we observed reliable cell capture and reduced cell deformation, with a 92% average recovery rate and 351 peripheral blood leukocytes (PBL) per millilitre (average). We expect the SSA-MOA platform to optimize CTC recovery rates, purity, and stability, increasing the sensitivity and reliability of such tests, thereby potentially expanding the utilization of CTC technologies in the clinic. 相似文献
68.
Lee S Kim J In S Choi H Oh SM Jang CG Chung KH 《Analytical and bioanalytical chemistry》2012,403(5):1385-1394
Owing to the tight control of methamphetamine, it is presumed that phentermine, an amphetamine-type anorectic, has recently
been considered a supplement for methamphetamine abusers in Korea. In addition, the abuse of other anorectics obtained by
inappropriate means has become a social issue. Hair is a useful specimen to prove chronic drug use. Therefore, an analytical
method for the simultaneous detection of phentermine, phendimetrazine, amfepramone, fenfluramine, mazindol, methamphetamine,
and 3,4-methylenedioxymethamphetamine (MDMA), as well as their metabolites, which covers the major amphetamines and anorectic
agents in Korea, in hair was established and validated using liquid chromatography–tandem mass spectrometry (LC-MS/MS). The
drugs and their metabolites in hair were extracted using 1 % HCl in methanol and then filtered and analyzed by LC-MS/MS with
electrospray ionization in positive mode. The validation results for selectivity, linearity, matrix effect, recovery, process
efficiency, intra- and interassay precision and accuracy, and processed sample stability were satisfactory. The limits of
detection ranged from 0.025 to 1 ng/10 mg hair and the limits of quantification were 0.25 ng/10 mg hair for every analyte
except mazindol and phentermine, for which they were 10 ng/10 mg hair. The method was successfully applied for the segmental
determination of selected anorectics, methamphetamine, MDMA, and their metabolites in hair from 39 drug suspects. Among the
anorectics, phentermine and/or phendimetrazine were identified with or without methamphetamine in the hair samples. Closer
supervision of the inappropriate use of anorectics is necessary. Also, hair analysis is useful for monitoring the abuse potential
of unnoticed drugs. 相似文献
69.
A m-xylene bridged imidazolium receptor 1 has been designed and synthesized. The receptor 1 utilizes two imidazole (C–H)+—anion hydrogen bonds and one aromatic hydrogen—anion hydrogen bond. The major driving force of complexation between the receptor 1 and anions comes from two imidazole (C–H)+—anion hydrogen bonding. However, some hydrogen bonding energy between aromatic hydrogen and anion exists, although it is expected to be much smaller than that of imidazole (C–H)+—anion hydrogen bonds. 相似文献
70.
Richard A. Bartsch Takashi Hayashita Joung Hae Lee Jong Seung Kim Matthew G. Hankins 《Supramolecular chemistry》2013,25(3-4):305-311
Abstract Lipophilic crown ethers with pendent proton-ionizable groups are novel complexing agents for use in metal ion separations by solvent extraction. For a series of structurally related, lipophilic dibenzocrown ether carboxylic acids, the efficiency and selectivity of competitive alkali metal cation extraction for aqueous solution into chloroform is found to be strongly influenced by the crown ether ring size and the lipophilic group attachment site. Reaction of dibenzocrown ether carboxylic acids with formaldehyde in formic acid produces condensation polymers which possess both ion-exchange and cyclic polyether binding sites for metal ion complexation. These resins exhibit excellent exchange kinetics for competitive alkali metal cation sorption from aqueous solution and subsequent stripping and may be used in concentrator columns for the recovery of these metal ions from very dilute aqueous solution. Cation selectivity in the sorption and stripping steps is controlled by the structure of the crown ether monomer unit. 相似文献