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Patchy micelles based on coassembly of block copolymer chains and block copolymer brushes on silica particles.

Langmuir : the ACS journal of surfaces and colloids

Zhu S, Li ZW, Zhao H.
PMID: 25811763
Langmuir. 2015 Apr 14;31(14):4129-36. doi: 10.1021/acs.langmuir.5b00526. Epub 2015 Apr 01.

Patchy particles are a type of colloidal particles with one or more well-defined patches on the surfaces. The patchy particles with multiple compositions and functionalities have found wide applications from the fundamental studies to practical uses. In this research...

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Zhu S, Li ZW, Zhao H. Patchy micelles based on coassembly of block copolymer chains and block copolymer brushes on silica particles. Langmuir. 2015;31(14):4129-36doi: 10.1021/acs.langmuir.5b00526.
Zhu, S., Li, Z. W., & Zhao, H. (2015). Patchy micelles based on coassembly of block copolymer chains and block copolymer brushes on silica particles. Langmuir : the ACS journal of surfaces and colloids, 31(14), 4129-36. https://doi.org/10.1021/acs.langmuir.5b00526
Zhu, Shuzhe, et al. "Patchy micelles based on coassembly of block copolymer chains and block copolymer brushes on silica particles." Langmuir : the ACS journal of surfaces and colloids vol. 31,14 (2015): 4129-36. doi: https://doi.org/10.1021/acs.langmuir.5b00526
Zhu S, Li ZW, Zhao H. Patchy micelles based on coassembly of block copolymer chains and block copolymer brushes on silica particles. Langmuir. 2015 Apr 14;31(14):4129-36. doi: 10.1021/acs.langmuir.5b00526. Epub 2015 Apr 01. PMID: 25811763.
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Transfer-Free Growth of Atomically Thin Transition Metal Disulfides Using a Solution Precursor by a Laser Irradiation Process and Their Application in Low-Power Photodetectors.

Nano letters

Huang CC, Medina H, Chen YZ, Su TY, Li JG, Chen CW, Yen YT, Wang ZM, Chueh YL.
PMID: 26906714
Nano Lett. 2016 Apr 13;16(4):2463-70. doi: 10.1021/acs.nanolett.6b00033. Epub 2016 Mar 21.

Although chemical vapor deposition is the most common method to synthesize transition metal dichalcogenides (TMDs), several obstacles, such as the high annealing temperature restricting the substrates used in the process and the required transfer causing the formation of wrinkles...

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Huang CC, Medina H, Chen YZ, et al. Transfer-Free Growth of Atomically Thin Transition Metal Disulfides Using a Solution Precursor by a Laser Irradiation Process and Their Application in Low-Power Photodetectors. Nano Lett. 2016;16(4):2463-70doi: 10.1021/acs.nanolett.6b00033.
Huang, C. C., Medina, H., Chen, Y. Z., Su, T. Y., Li, J. G., Chen, C. W., Yen, Y. T., Wang, Z. M., & Chueh, Y. L. (2016). Transfer-Free Growth of Atomically Thin Transition Metal Disulfides Using a Solution Precursor by a Laser Irradiation Process and Their Application in Low-Power Photodetectors. Nano letters, 16(4), 2463-70. https://doi.org/10.1021/acs.nanolett.6b00033
Huang, Chi-Chih, et al. "Transfer-Free Growth of Atomically Thin Transition Metal Disulfides Using a Solution Precursor by a Laser Irradiation Process and Their Application in Low-Power Photodetectors." Nano letters vol. 16,4 (2016): 2463-70. doi: https://doi.org/10.1021/acs.nanolett.6b00033
Huang CC, Medina H, Chen YZ, Su TY, Li JG, Chen CW, Yen YT, Wang ZM, Chueh YL. Transfer-Free Growth of Atomically Thin Transition Metal Disulfides Using a Solution Precursor by a Laser Irradiation Process and Their Application in Low-Power Photodetectors. Nano Lett. 2016 Apr 13;16(4):2463-70. doi: 10.1021/acs.nanolett.6b00033. Epub 2016 Mar 21. PMID: 26906714.
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Redox regulation by reversible protein S-thiolation in bacteria.

Frontiers in microbiology

Loi VV, Rossius M, Antelmann H.
PMID: 25852656
Front Microbiol. 2015 Mar 16;6:187. doi: 10.3389/fmicb.2015.00187. eCollection 2015.

Low molecular weight (LMW) thiols function as thiol-redox buffers to maintain the reduced state of the cytoplasm. The best studied LMW thiol is the tripeptide glutathione (GSH) present in all eukaryotes and Gram-negative bacteria. Firmicutes bacteria, including Bacillus and...

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Loi VV, Rossius M, Antelmann H. Redox regulation by reversible protein S-thiolation in bacteria. Front Microbiol. 2015;6:187doi: 10.3389/fmicb.2015.00187.
Loi, V. V., Rossius, M., & Antelmann, H. (2015). Redox regulation by reversible protein S-thiolation in bacteria. Frontiers in microbiology, 6187. https://doi.org/10.3389/fmicb.2015.00187
Loi, Vu Van, et al. "Redox regulation by reversible protein S-thiolation in bacteria." Frontiers in microbiology vol. 6 (2015): 187. doi: https://doi.org/10.3389/fmicb.2015.00187
Loi VV, Rossius M, Antelmann H. Redox regulation by reversible protein S-thiolation in bacteria. Front Microbiol. 2015 Mar 16;6:187. doi: 10.3389/fmicb.2015.00187. eCollection 2015. PMID: 25852656; PMCID: PMC4360819.
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Preparation of difluoromethylthioethers through difluoromethylation of disulfides using TMS-CF2H.

Chemical communications (Cambridge, England)

Howard JL, Schotten C, Alston ST, Browne DL.
PMID: 27306975
Chem Commun (Camb). 2016 Jun 28;52(54):8448-51. doi: 10.1039/c6cc02693a.

We report an operationally simple, metal-free approach for the late-stage introduction of the important lipophilic hydrogen-bond donor motif, SCF2H. This reaction converts diaryl- and dialkyl-disulfides into the corresponding aryl/alkyl-SCF2H through the nucleophilic transfer of a difluoromethyl group with good...

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Howard JL, Schotten C, Alston ST, et al. Preparation of difluoromethylthioethers through difluoromethylation of disulfides using TMS-CF2H. Chem Commun (Camb). 2016;52(54):8448-51doi: 10.1039/c6cc02693a.
Howard, J. L., Schotten, C., Alston, S. T., & Browne, D. L. (2016). Preparation of difluoromethylthioethers through difluoromethylation of disulfides using TMS-CF2H. Chemical communications (Cambridge, England), 52(54), 8448-51. https://doi.org/10.1039/c6cc02693a
Howard, Joseph L, et al. "Preparation of difluoromethylthioethers through difluoromethylation of disulfides using TMS-CF2H." Chemical communications (Cambridge, England) vol. 52,54 (2016): 8448-51. doi: https://doi.org/10.1039/c6cc02693a
Howard JL, Schotten C, Alston ST, Browne DL. Preparation of difluoromethylthioethers through difluoromethylation of disulfides using TMS-CF2H. Chem Commun (Camb). 2016 Jun 28;52(54):8448-51. doi: 10.1039/c6cc02693a. PMID: 27306975.
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Addition reaction of dialkyl disulfides to terminal alkynes catalyzed by a rhodium complex and trifluoromethanesulfonic acid.

Organic letters

Arisawa M, Yamaguchi M.
PMID: 11259056
Org Lett. 2001 Mar 08;3(5):763-4. doi: 10.1021/ol015521l.

[reaction: see text]. Addition of dialkyl disulfides to terminal alkynes is catalyzed by a rhodium-phosphine complex and trifluoromethanesulfonic acid giving (Z)-bis(alkylthio)olefins stereoselectively.

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Arisawa M, Yamaguchi M. Addition reaction of dialkyl disulfides to terminal alkynes catalyzed by a rhodium complex and trifluoromethanesulfonic acid. Org Lett. 2001;3(5):763-4doi: 10.1021/ol015521l.
Arisawa, M., & Yamaguchi, M. (2001). Addition reaction of dialkyl disulfides to terminal alkynes catalyzed by a rhodium complex and trifluoromethanesulfonic acid. Organic letters, 3(5), 763-4. https://doi.org/10.1021/ol015521l
Arisawa, M, and Yamaguchi, M. "Addition reaction of dialkyl disulfides to terminal alkynes catalyzed by a rhodium complex and trifluoromethanesulfonic acid." Organic letters vol. 3,5 (2001): 763-4. doi: https://doi.org/10.1021/ol015521l
Arisawa M, Yamaguchi M. Addition reaction of dialkyl disulfides to terminal alkynes catalyzed by a rhodium complex and trifluoromethanesulfonic acid. Org Lett. 2001 Mar 08;3(5):763-4. doi: 10.1021/ol015521l. PMID: 11259056.
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Kinetics and Equilibria of the Thiol/Disulfide Exchange Reactions of Somatostatin with Glutathione.

The Journal of organic chemistry

Rabenstein DL, Weaver KH.
PMID: 11667665
J Org Chem. 1996 Oct 18;61(21):7391-7397. doi: 10.1021/jo960917+.

Rate and equilibrium constants are reported for the thiol/disulfide exchange reactions of the peptide hormone somatostatin with glutathione (GSH). GSH reacts with the disulfide bond of somatostatin to form somatostatin-glutathione mixed disulfides (Cys(3)-SH, Cys(14)-SSG and Cys(3)-SSG, Cys(14)-SH), each of...

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Rabenstein DL, Weaver KH. Kinetics and Equilibria of the Thiol/Disulfide Exchange Reactions of Somatostatin with Glutathione. J Org Chem. 1996;61(21):7391-7397doi: 10.1021/jo960917+.
Rabenstein, D. L., & Weaver, K. H. (1996). Kinetics and Equilibria of the Thiol/Disulfide Exchange Reactions of Somatostatin with Glutathione. The Journal of organic chemistry, 61(21), 7391-7397. https://doi.org/10.1021/jo960917+
Rabenstein, Dallas L., and Weaver, Kim H.. "Kinetics and Equilibria of the Thiol/Disulfide Exchange Reactions of Somatostatin with Glutathione." The Journal of organic chemistry vol. 61,21 (1996): 7391-7397. doi: https://doi.org/10.1021/jo960917+
Rabenstein DL, Weaver KH. Kinetics and Equilibria of the Thiol/Disulfide Exchange Reactions of Somatostatin with Glutathione. J Org Chem. 1996 Oct 18;61(21):7391-7397. doi: 10.1021/jo960917+. PMID: 11667665.
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Ligand-stabilized ruthenium nanoparticles: synthesis, organization, and dynamics.

Journal of the American Chemical Society

Pan C, Pelzer K, Philippot K, Chaudret B, Dassenoy F, Lecante P, Casanove MJ.
PMID: 11480979
J Am Chem Soc. 2001 Aug 08;123(31):7584-93. doi: 10.1021/ja003961m.

The decomposition of the ruthenium precursor Ru(COD)(COT) (1, COD = 1,5-cyclooctadiene; COT = 1,3,5-cyclooctatriene) in mild conditions (room temperature, 1--3 bar H(2)) in THF leads, in the presence of a stabilizer (polymer or ligand), to nanoparticles of various sizes...

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Pan C, Pelzer K, Philippot K, et al. Ligand-stabilized ruthenium nanoparticles: synthesis, organization, and dynamics. J Am Chem Soc. 2001;123(31):7584-93doi: 10.1021/ja003961m.
Pan, C., Pelzer, K., Philippot, K., Chaudret, B., Dassenoy, F., Lecante, P., & Casanove, M. J. (2001). Ligand-stabilized ruthenium nanoparticles: synthesis, organization, and dynamics. Journal of the American Chemical Society, 123(31), 7584-93. https://doi.org/10.1021/ja003961m
Pan, C, et al. "Ligand-stabilized ruthenium nanoparticles: synthesis, organization, and dynamics." Journal of the American Chemical Society vol. 123,31 (2001): 7584-93. doi: https://doi.org/10.1021/ja003961m
Pan C, Pelzer K, Philippot K, Chaudret B, Dassenoy F, Lecante P, Casanove MJ. Ligand-stabilized ruthenium nanoparticles: synthesis, organization, and dynamics. J Am Chem Soc. 2001 Aug 08;123(31):7584-93. doi: 10.1021/ja003961m. PMID: 11480979.
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A Novel Class of Conformationally Constrained, Masked Cysteines: Synthesis of 2-Alkyl- and 2-Arylsulfanyl-1-aminocyclopropanecarboxylic Acids.

The Journal of organic chemistry

Clerici F, Gelmi ML, Pocar D.
PMID: 11674139
J Org Chem. 1999 Feb 05;64(3):726-730. doi: 10.1021/jo9810011.

A convenient synthesis of 4-sulfanylmethylene-5(4H)-oxazolones 3 was realized starting from 4-(chloromethylene)oxazolone 1 and mercaptans 2. Oxazolones 3 were used as starting materials for the preparation of unknown 2-sulfanyl-1-aminocyclopropanecarboxylic acid derivatives 5 and7. Oxazolones 3 were cyclopropanated at the exocyclic...

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Clerici F, Gelmi ML, Pocar D. A Novel Class of Conformationally Constrained, Masked Cysteines: Synthesis of 2-Alkyl- and 2-Arylsulfanyl-1-aminocyclopropanecarboxylic Acids. J Org Chem. 1999;64(3):726-730doi: 10.1021/jo9810011.
Clerici, F., Gelmi, M. L., & Pocar, D. (1999). A Novel Class of Conformationally Constrained, Masked Cysteines: Synthesis of 2-Alkyl- and 2-Arylsulfanyl-1-aminocyclopropanecarboxylic Acids. The Journal of organic chemistry, 64(3), 726-730. https://doi.org/10.1021/jo9810011
Clerici, F., et al. "A Novel Class of Conformationally Constrained, Masked Cysteines: Synthesis of 2-Alkyl- and 2-Arylsulfanyl-1-aminocyclopropanecarboxylic Acids." The Journal of organic chemistry vol. 64,3 (1999): 726-730. doi: https://doi.org/10.1021/jo9810011
Clerici F, Gelmi ML, Pocar D. A Novel Class of Conformationally Constrained, Masked Cysteines: Synthesis of 2-Alkyl- and 2-Arylsulfanyl-1-aminocyclopropanecarboxylic Acids. J Org Chem. 1999 Feb 05;64(3):726-730. doi: 10.1021/jo9810011. PMID: 11674139.
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1,4-Naphthoquinone Disulfides and Methyl Sulfides: Self-Assembled Monolayers on Gold Substrates.

The Journal of organic chemistry

Panetta CA, Fan PW, Fattah R, Greever JC, He Z, Hussey CL, Sha D, Wescott LD.
PMID: 11674367
J Org Chem. 1999 Apr 16;64(8):2919-2923. doi: 10.1021/jo981185j.

No abstract available.

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Panetta CA, Fan PW, Fattah R, et al. 1,4-Naphthoquinone Disulfides and Methyl Sulfides: Self-Assembled Monolayers on Gold Substrates. J Org Chem. 1999;64(8):2919-2923doi: 10.1021/jo981185j.
Panetta, C. A., Fan, P. W., Fattah, R., Greever, J. C., He, Z., Hussey, C. L., Sha, D., & Wescott, L. D. (1999). 1,4-Naphthoquinone Disulfides and Methyl Sulfides: Self-Assembled Monolayers on Gold Substrates. The Journal of organic chemistry, 64(8), 2919-2923. https://doi.org/10.1021/jo981185j
Panetta, Charles A., et al. "1,4-Naphthoquinone Disulfides and Methyl Sulfides: Self-Assembled Monolayers on Gold Substrates." The Journal of organic chemistry vol. 64,8 (1999): 2919-2923. doi: https://doi.org/10.1021/jo981185j
Panetta CA, Fan PW, Fattah R, Greever JC, He Z, Hussey CL, Sha D, Wescott LD. 1,4-Naphthoquinone Disulfides and Methyl Sulfides: Self-Assembled Monolayers on Gold Substrates. J Org Chem. 1999 Apr 16;64(8):2919-2923. doi: 10.1021/jo981185j. PMID: 11674367.
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Self-Assembled Monolayers of Organoselenium Compounds on Gold: Surface-Enhanced Raman Scattering Study.

Journal of colloid and interface science

Han SW, Kim K.
PMID: 11482958
J Colloid Interface Sci. 2001 Aug 15;240(2):492-497. doi: 10.1006/jcis.2001.7702.

To understand the binding nature of organoselenium compounds on gold, we have examined the adsorption behavior of several representative organoselenium compounds, i.e., benzeneselenol (BSe), diphenyl diselenide, dibenzyl diselenide, dioctyl diselenide, and benzyl phenyl selenide (BPSe) on the Au surface...

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Han SW, Kim K. Self-Assembled Monolayers of Organoselenium Compounds on Gold: Surface-Enhanced Raman Scattering Study. J Colloid Interface Sci. 2001;240(2):492-497doi: 10.1006/jcis.2001.7702.
Han, S. W., & Kim, K. (2001). Self-Assembled Monolayers of Organoselenium Compounds on Gold: Surface-Enhanced Raman Scattering Study. Journal of colloid and interface science, 240(2), 492-497. https://doi.org/10.1006/jcis.2001.7702
Han, Sang Woo, and Kim, Kwan. "Self-Assembled Monolayers of Organoselenium Compounds on Gold: Surface-Enhanced Raman Scattering Study." Journal of colloid and interface science vol. 240,2 (2001): 492-497. doi: https://doi.org/10.1006/jcis.2001.7702
Han SW, Kim K. Self-Assembled Monolayers of Organoselenium Compounds on Gold: Surface-Enhanced Raman Scattering Study. J Colloid Interface Sci. 2001 Aug 15;240(2):492-497. doi: 10.1006/jcis.2001.7702. PMID: 11482958.
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Direct synthesis of mesostructured lamellar molybdenum disulfides using a molten neutral n-alkylamine as the solvent and template.

Journal of the American Chemical Society

Vanchura BA, He P, Antochshuk V, Jaroniec M, Ferryman A, Barbash D, Fulghum JE, Huang SD.
PMID: 12371837
J Am Chem Soc. 2002 Oct 16;124(41):12090-1. doi: 10.1021/ja025786a.

A series of novel mesostructured lamellar molybdenum disulfides with the d spacings from 17 to 30 A can be prepared by the reaction of Mo(CO)6 with elemental sulfur using a molten n-alkylamine as the solvent as well as the...

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Vanchura BA, He P, Antochshuk V, et al. Direct synthesis of mesostructured lamellar molybdenum disulfides using a molten neutral n-alkylamine as the solvent and template. J Am Chem Soc. 2002;124(41):12090-1doi: 10.1021/ja025786a.
Vanchura, B. A., He, P., Antochshuk, V., Jaroniec, M., Ferryman, A., Barbash, D., Fulghum, J. E., & Huang, S. D. (2002). Direct synthesis of mesostructured lamellar molybdenum disulfides using a molten neutral n-alkylamine as the solvent and template. Journal of the American Chemical Society, 124(41), 12090-1. https://doi.org/10.1021/ja025786a
Vanchura, Britt A, et al. "Direct synthesis of mesostructured lamellar molybdenum disulfides using a molten neutral n-alkylamine as the solvent and template." Journal of the American Chemical Society vol. 124,41 (2002): 12090-1. doi: https://doi.org/10.1021/ja025786a
Vanchura BA, He P, Antochshuk V, Jaroniec M, Ferryman A, Barbash D, Fulghum JE, Huang SD. Direct synthesis of mesostructured lamellar molybdenum disulfides using a molten neutral n-alkylamine as the solvent and template. J Am Chem Soc. 2002 Oct 16;124(41):12090-1. doi: 10.1021/ja025786a. PMID: 12371837.
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Auxin-Modulated Protein Disulfide-Thiol-Interchange Activity from Soybean Plasma Membranes.

Plant physiology

Morre DJ, De Cabo R, Jacobs E, Morre DM.
PMID: 12228613
Plant Physiol. 1995 Oct;109(2):573-578. doi: 10.1104/pp.109.2.573.

The renaturation of scrambled (oxidized and inactive) RNase A is catalyzed by soybean (Glycine max cv Williams 82) plasma membranes. The catalysis is stimulated by the auxin herbicide 2,4-dichlorophenoxyacetic acid or by the natural auxin indole-3-acetic acid. The inactive...

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Morre DJ, De Cabo R, Jacobs E, et al. Auxin-Modulated Protein Disulfide-Thiol-Interchange Activity from Soybean Plasma Membranes. Plant Physiol. 1995;109(2):573-578doi: 10.1104/pp.109.2.573.
Morre, D. J., De Cabo, R., Jacobs, E., & Morre, D. M. (1995). Auxin-Modulated Protein Disulfide-Thiol-Interchange Activity from Soybean Plasma Membranes. Plant physiology, 109(2), 573-578. https://doi.org/10.1104/pp.109.2.573
Morre, D. J., et al. "Auxin-Modulated Protein Disulfide-Thiol-Interchange Activity from Soybean Plasma Membranes." Plant physiology vol. 109,2 (1995): 573-578. doi: https://doi.org/10.1104/pp.109.2.573
Morre DJ, De Cabo R, Jacobs E, Morre DM. Auxin-Modulated Protein Disulfide-Thiol-Interchange Activity from Soybean Plasma Membranes. Plant Physiol. 1995 Oct;109(2):573-578. doi: 10.1104/pp.109.2.573. PMID: 12228613; PMCID: PMC157622.
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Showing 13 to 24 of 588 entries