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Surface diagnostics of evaporating droplets of nanosphere suspension: Fano interference and surface pressure.

Physical chemistry chemical physics : PCCP

Kolwas M, Kolwas K, Derkachov G, Jakubczyk D.
PMID: 25673315
Phys Chem Chem Phys. 2015 Mar 14;17(10):6881-8. doi: 10.1039/c5cp00013k.

The evaporation of a single, levitating microdroplet of glycols containing SiO2 nanospheres, both of similar refraction indices, was studied by observing changes in the interference pattern and intensities of polarized and depolarized scattered laser light. The evolution of the...

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Kolwas M, Kolwas K, Derkachov G, et al. Surface diagnostics of evaporating droplets of nanosphere suspension: Fano interference and surface pressure. Phys Chem Chem Phys. 2015;17(10):6881-8doi: 10.1039/c5cp00013k.
Kolwas, M., Kolwas, K., Derkachov, G., & Jakubczyk, D. (2015). Surface diagnostics of evaporating droplets of nanosphere suspension: Fano interference and surface pressure. Physical chemistry chemical physics : PCCP, 17(10), 6881-8. https://doi.org/10.1039/c5cp00013k
Kolwas, Maciej, et al. "Surface diagnostics of evaporating droplets of nanosphere suspension: Fano interference and surface pressure." Physical chemistry chemical physics : PCCP vol. 17,10 (2015): 6881-8. doi: https://doi.org/10.1039/c5cp00013k
Kolwas M, Kolwas K, Derkachov G, Jakubczyk D. Surface diagnostics of evaporating droplets of nanosphere suspension: Fano interference and surface pressure. Phys Chem Chem Phys. 2015 Mar 14;17(10):6881-8. doi: 10.1039/c5cp00013k. PMID: 25673315.
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Two open states of P2X receptor channels.

Frontiers in cellular neuroscience

Rokic MB, Stojilkovic SS.
PMID: 24312007
Front Cell Neurosci. 2013 Nov 14;7:215. doi: 10.3389/fncel.2013.00215.

The occupancy of the orthosteric ligand binding sites of P2X receptor (P2XR) channels causes the rapid opening of a small cation-permeable pore, followed by a gradual dilation that renders the pore permeable to large organic cations. Electrophysiologically, this phenomenon...

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Rokic MB, Stojilkovic SS. Two open states of P2X receptor channels. Front Cell Neurosci. 2013;7:215doi: 10.3389/fncel.2013.00215.
Rokic, M. B., & Stojilkovic, S. S. (2013). Two open states of P2X receptor channels. Frontiers in cellular neuroscience, 7215. https://doi.org/10.3389/fncel.2013.00215
Rokic, Milos B, and Stojilkovic, Stanko S. "Two open states of P2X receptor channels." Frontiers in cellular neuroscience vol. 7 (2013): 215. doi: https://doi.org/10.3389/fncel.2013.00215
Rokic MB, Stojilkovic SS. Two open states of P2X receptor channels. Front Cell Neurosci. 2013 Nov 14;7:215. doi: 10.3389/fncel.2013.00215. PMID: 24312007; PMCID: PMC3834609.
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Organic soluble and uniform film forming oligoethylene glycol substituted BODIPY small molecules with improved hole mobility.

Physical chemistry chemical physics : PCCP

Singh S, Venugopalan V, Krishnamoorthy K.
PMID: 24874914
Phys Chem Chem Phys. 2014 Jul 14;16(26):13376-82. doi: 10.1039/c4cp01098a.

Judiciously chosen side chains of conjugated molecules have a positive impact on charge transport properties when used as the active material in organic electronic devices. Amongst the side chains, oligoethylene glycols (OEGs) have been relatively unexplored due to their...

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Singh S, Venugopalan V, Krishnamoorthy K. Organic soluble and uniform film forming oligoethylene glycol substituted BODIPY small molecules with improved hole mobility. Phys Chem Chem Phys. 2014;16(26):13376-82doi: 10.1039/c4cp01098a.
Singh, S., Venugopalan, V., & Krishnamoorthy, K. (2014). Organic soluble and uniform film forming oligoethylene glycol substituted BODIPY small molecules with improved hole mobility. Physical chemistry chemical physics : PCCP, 16(26), 13376-82. https://doi.org/10.1039/c4cp01098a
Singh, Saumya, et al. "Organic soluble and uniform film forming oligoethylene glycol substituted BODIPY small molecules with improved hole mobility." Physical chemistry chemical physics : PCCP vol. 16,26 (2014): 13376-82. doi: https://doi.org/10.1039/c4cp01098a
Singh S, Venugopalan V, Krishnamoorthy K. Organic soluble and uniform film forming oligoethylene glycol substituted BODIPY small molecules with improved hole mobility. Phys Chem Chem Phys. 2014 Jul 14;16(26):13376-82. doi: 10.1039/c4cp01098a. PMID: 24874914.
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Leveling effects of ammonium salts on thermal stabilities of polyethylene glycols.

Soft matter

Xia J, Song le X, Liu W, Teng Y.
PMID: 26029781
Soft Matter. 2013 Oct 28;9(40):9714-22. doi: 10.1039/c3sm51484f.

In this work, the thermal stabilities of a series of polyethylene glycols (PEG 4000, 6000 and 10000) were investigated after compositing with different kinds of inorganic salts, such as ammonium molybdate tetrahydrate (AMT), NH4VO3, (NH4)2SO4, NH4NO3, Na2SO4, Na2MoO4. It...

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Xia J, Song le X, Liu W, et al. Leveling effects of ammonium salts on thermal stabilities of polyethylene glycols. Soft Matter. 2013;9(40):9714-22doi: 10.1039/c3sm51484f.
Xia, J., Song, l. e. . X., Liu, W., & Teng, Y. (2013). Leveling effects of ammonium salts on thermal stabilities of polyethylene glycols. Soft matter, 9(40), 9714-22. https://doi.org/10.1039/c3sm51484f
Xia, Juan, et al. "Leveling effects of ammonium salts on thermal stabilities of polyethylene glycols." Soft matter vol. 9,40 (2013): 9714-22. doi: https://doi.org/10.1039/c3sm51484f
Xia J, Song le X, Liu W, Teng Y. Leveling effects of ammonium salts on thermal stabilities of polyethylene glycols. Soft Matter. 2013 Oct 28;9(40):9714-22. doi: 10.1039/c3sm51484f. PMID: 26029781.
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Long-Term Safety of PEGylated Coagulation Factor VIII in the Immune-Deficient Rowett Nude Rat.

Journal of toxicology

Rasmussen CE, Nowak J, Larsen JM, Moore E, Bell D, Liu KC, Sorensen NS, Kappers WA, Krogh-Meibom T, Offenberg H.
PMID: 28458688
J Toxicol. 2017;2017:8496246. doi: 10.1155/2017/8496246. Epub 2017 Mar 28.

Turoctocog alfa pegol (N8-GP) is a glycoPEGylated human recombinant factor VIII for the treatment of hemophilia A. The safety profile of rFVIII, and polyethylene glycols (PEG) technology, is well-established. Conducting long-term toxicity studies in animals using human proteins can...

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Rasmussen CE, Nowak J, Larsen JM, et al. Long-Term Safety of PEGylated Coagulation Factor VIII in the Immune-Deficient Rowett Nude Rat. J Toxicol. 2017;2017:8496246doi: 10.1155/2017/8496246.
Rasmussen, C. E., Nowak, J., Larsen, J. M., Moore, E., Bell, D., Liu, K. C., Sorensen, N. S., Kappers, W. A., Krogh-Meibom, T., & Offenberg, H. (2017). Long-Term Safety of PEGylated Coagulation Factor VIII in the Immune-Deficient Rowett Nude Rat. Journal of toxicology, 20178496246. https://doi.org/10.1155/2017/8496246
Rasmussen, Caroline E, et al. "Long-Term Safety of PEGylated Coagulation Factor VIII in the Immune-Deficient Rowett Nude Rat." Journal of toxicology vol. 2017 (2017): 8496246. doi: https://doi.org/10.1155/2017/8496246
Rasmussen CE, Nowak J, Larsen JM, Moore E, Bell D, Liu KC, Sorensen NS, Kappers WA, Krogh-Meibom T, Offenberg H. Long-Term Safety of PEGylated Coagulation Factor VIII in the Immune-Deficient Rowett Nude Rat. J Toxicol. 2017;2017:8496246. doi: 10.1155/2017/8496246. Epub 2017 Mar 28. PMID: 28458688; PMCID: PMC5387834.
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Reduction and control of domain spacing by additive inclusion: morphology and orientation effects of glycols on microphase separated PS-b-PEO.

Journal of colloid and interface science

Ghoshal T, Shaw MT, Holmes JD, Morris MA.
PMID: 25814102
J Colloid Interface Sci. 2015 Jul 15;450:141-150. doi: 10.1016/j.jcis.2015.03.022. Epub 2015 Mar 17.

Cylindrical phase polystyrene-b-polyethylene oxide (PS-b-PEO) block copolymer (BCP) was combined with lower molecular weight poly/ethylene glycols at different concentrations and their effect on the microphase separation of BCP thin films were studied. Well-ordered microphase separated, periodic nanostructures were realized...

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Ghoshal T, Shaw MT, Holmes JD, et al. Reduction and control of domain spacing by additive inclusion: morphology and orientation effects of glycols on microphase separated PS-b-PEO. J Colloid Interface Sci. 2015;450:141-150doi: 10.1016/j.jcis.2015.03.022.
Ghoshal, T., Shaw, M. T., Holmes, J. D., & Morris, M. A. (2015). Reduction and control of domain spacing by additive inclusion: morphology and orientation effects of glycols on microphase separated PS-b-PEO. Journal of colloid and interface science, 450141-150. https://doi.org/10.1016/j.jcis.2015.03.022
Ghoshal, Tandra, et al. "Reduction and control of domain spacing by additive inclusion: morphology and orientation effects of glycols on microphase separated PS-b-PEO." Journal of colloid and interface science vol. 450 (2015): 141-150. doi: https://doi.org/10.1016/j.jcis.2015.03.022
Ghoshal T, Shaw MT, Holmes JD, Morris MA. Reduction and control of domain spacing by additive inclusion: morphology and orientation effects of glycols on microphase separated PS-b-PEO. J Colloid Interface Sci. 2015 Jul 15;450:141-150. doi: 10.1016/j.jcis.2015.03.022. Epub 2015 Mar 17. PMID: 25814102.
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A rapid analysis of plasma/serum ethylene and propylene glycol by headspace gas chromatography.

SpringerPlus

Ehlers A, Morris C, Krasowski MD.
PMID: 23741644
Springerplus. 2013 May 01;2(1):203. doi: 10.1186/2193-1801-2-203. Print 2013 Dec.

A rapid headspace-gas chromatography (HS-GC) method was developed for the analysis of ethylene glycol and propylene glycol in plasma and serum specimens using 1,3-propanediol as the internal standard. The method employed a single-step derivitization using phenylboronic acid, was linear...

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Ehlers A, Morris C, Krasowski MD. A rapid analysis of plasma/serum ethylene and propylene glycol by headspace gas chromatography. Springerplus. 2013;2(1):203doi: 10.1186/2193-1801-2-203.
Ehlers, A., Morris, C., & Krasowski, M. D. (2013). A rapid analysis of plasma/serum ethylene and propylene glycol by headspace gas chromatography. SpringerPlus, 2(1), 203. https://doi.org/10.1186/2193-1801-2-203
Ehlers, Alexandra, et al. "A rapid analysis of plasma/serum ethylene and propylene glycol by headspace gas chromatography." SpringerPlus vol. 2,1 (2013): 203. doi: https://doi.org/10.1186/2193-1801-2-203
Ehlers A, Morris C, Krasowski MD. A rapid analysis of plasma/serum ethylene and propylene glycol by headspace gas chromatography. Springerplus. 2013 May 01;2(1):203. doi: 10.1186/2193-1801-2-203. Print 2013 Dec. PMID: 23741644; PMCID: PMC3667371.
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Transport Properties of Cation Exchange Membranes in the Presence of Ether Compounds in Electrodialysis.

Journal of colloid and interface science

Sata T, Tanimoto M, Kawamura K, Matsusaki K.
PMID: 10534389
J Colloid Interface Sci. 1999 Nov 15;219(2):310-319. doi: 10.1006/jcis.1999.6482.

Ether compounds such as ethylene glycols with different molecular weights and crown ethers have good affinity to the cation exchange membranes, sulfonated styrene-divinylbenzene membrane (sodium ion form) and perfluorocarbon sodium sulfonate membrane. The impregnated amount of ethylene glycols in...

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Sata T, Tanimoto M, Kawamura K, et al. Transport Properties of Cation Exchange Membranes in the Presence of Ether Compounds in Electrodialysis. J Colloid Interface Sci. 1999;219(2):310-319doi: 10.1006/jcis.1999.6482.
Sata, T., Tanimoto, M., Kawamura, K., & Matsusaki, K. (1999). Transport Properties of Cation Exchange Membranes in the Presence of Ether Compounds in Electrodialysis. Journal of colloid and interface science, 219(2), 310-319. https://doi.org/10.1006/jcis.1999.6482
Sata, et al. "Transport Properties of Cation Exchange Membranes in the Presence of Ether Compounds in Electrodialysis." Journal of colloid and interface science vol. 219,2 (1999): 310-319. doi: https://doi.org/10.1006/jcis.1999.6482
Sata T, Tanimoto M, Kawamura K, Matsusaki K. Transport Properties of Cation Exchange Membranes in the Presence of Ether Compounds in Electrodialysis. J Colloid Interface Sci. 1999 Nov 15;219(2):310-319. doi: 10.1006/jcis.1999.6482. PMID: 10534389.
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A linear relation between the cloud point and the number of oxyethylene units of water-soluble nonionic surfactants valid for the entire range of ethoxylation.

Journal of colloid and interface science

Schott H.
PMID: 12742053
J Colloid Interface Sci. 2003 Apr 01;260(1):219-24. doi: 10.1016/s0021-9797(02)00183-2.

The following linear equation correlates the cloud point (CP) of water-soluble polyoxyethylated nonionic surfactants (NSs) with the average number p of oxyethylene units per molecule: (p - p0)/CP = a + b(p - p0). Here p0 is the smallest...

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Schott H. A linear relation between the cloud point and the number of oxyethylene units of water-soluble nonionic surfactants valid for the entire range of ethoxylation. J Colloid Interface Sci. 2003;260(1):219-24doi: 10.1016/s0021-9797(02)00183-2.
Schott, H. (2003). A linear relation between the cloud point and the number of oxyethylene units of water-soluble nonionic surfactants valid for the entire range of ethoxylation. Journal of colloid and interface science, 260(1), 219-24. https://doi.org/10.1016/s0021-9797(02)00183-2
Schott, Hans. "A linear relation between the cloud point and the number of oxyethylene units of water-soluble nonionic surfactants valid for the entire range of ethoxylation." Journal of colloid and interface science vol. 260,1 (2003): 219-24. doi: https://doi.org/10.1016/s0021-9797(02)00183-2
Schott H. A linear relation between the cloud point and the number of oxyethylene units of water-soluble nonionic surfactants valid for the entire range of ethoxylation. J Colloid Interface Sci. 2003 Apr 01;260(1):219-24. doi: 10.1016/s0021-9797(02)00183-2. PMID: 12742053.
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Small-angle neutron scattering studies of aqueous solutions of short-chain amphiphiles.

The European physical journal. E, Soft matter

D'Arrigo G, Giordano R, Teixeira J.
PMID: 15011067
Eur Phys J E Soft Matter. 2003 Feb;10(2):135-42. doi: 10.1140/epje/e2003-00017-x.

We present small angle neutron scattering measurements on binary aqueous solutions of some short-chain amphiphiles (diols, triols, glycols and diglycols) at room temperature. The spectra were analysed in terms of the Teubner-Strey phenomenological formula which allows to obtain a...

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D'Arrigo G, Giordano R, Teixeira J. Small-angle neutron scattering studies of aqueous solutions of short-chain amphiphiles. Eur Phys J E Soft Matter. 2003;10(2):135-42doi: 10.1140/epje/e2003-00017-x.
D'Arrigo, G., Giordano, R., & Teixeira, J. (2003). Small-angle neutron scattering studies of aqueous solutions of short-chain amphiphiles. The European physical journal. E, Soft matter, 10(2), 135-42. https://doi.org/10.1140/epje/e2003-00017-x
D'Arrigo, G, et al. "Small-angle neutron scattering studies of aqueous solutions of short-chain amphiphiles." The European physical journal. E, Soft matter vol. 10,2 (2003): 135-42. doi: https://doi.org/10.1140/epje/e2003-00017-x
D'Arrigo G, Giordano R, Teixeira J. Small-angle neutron scattering studies of aqueous solutions of short-chain amphiphiles. Eur Phys J E Soft Matter. 2003 Feb;10(2):135-42. doi: 10.1140/epje/e2003-00017-x. PMID: 15011067.
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Role of defects in the nonmonotonic behavior of secondary relaxation of polypropylene glycols.

The Journal of chemical physics

Grzybowska K, Grzybowski A, Paluch M.
PMID: 18397104
J Chem Phys. 2008 Apr 07;128(13):134904. doi: 10.1063/1.2901045.

A nonmonotonic relaxation kinetic model [Ya. Ryabov et al., J. Phys. Chem. B 105, 1845 (2001)] is successfully applied to describe an intriguing slow down in the dielectric secondary gamma relaxation of polypropylene glycols (PPGs) with increasing temperature near...

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Grzybowska K, Grzybowski A, Paluch M. Role of defects in the nonmonotonic behavior of secondary relaxation of polypropylene glycols. J Chem Phys. 2008;128(13):134904doi: 10.1063/1.2901045.
Grzybowska, K., Grzybowski, A., & Paluch, M. (2008). Role of defects in the nonmonotonic behavior of secondary relaxation of polypropylene glycols. The Journal of chemical physics, 128(13), 134904. https://doi.org/10.1063/1.2901045
Grzybowska, K, et al. "Role of defects in the nonmonotonic behavior of secondary relaxation of polypropylene glycols." The Journal of chemical physics vol. 128,13 (2008): 134904. doi: https://doi.org/10.1063/1.2901045
Grzybowska K, Grzybowski A, Paluch M. Role of defects in the nonmonotonic behavior of secondary relaxation of polypropylene glycols. J Chem Phys. 2008 Apr 07;128(13):134904. doi: 10.1063/1.2901045. PMID: 18397104.
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Solvophobically-driven oligo(ethylene glycol) helical foldamers. Synthesis, characterization, and complexation with ethane-1,2-diaminium.

The Journal of organic chemistry

Hou JL, Jia MX, Jiang XK, Li ZT, Chen GJ.
PMID: 15357580
J Org Chem. 2004 Sep 17;69(19):6228-37. doi: 10.1021/jo049420n.

Oligo(ethylene glycols) 1a-h, which are incorporated with one to eight 2,3-naphthylene units, respectively, have been synthesized and characterized. The conformational changes of the new oligomers have been investigated in chloroform-acetonitrile binary solvents by the UV-vis, (1)H NMR, and fluorescent...

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Hou JL, Jia MX, Jiang XK, et al. Solvophobically-driven oligo(ethylene glycol) helical foldamers. Synthesis, characterization, and complexation with ethane-1,2-diaminium. J Org Chem. 2004;69(19):6228-37doi: 10.1021/jo049420n.
Hou, J. L., Jia, M. X., Jiang, X. K., Li, Z. T., & Chen, G. J. (2004). Solvophobically-driven oligo(ethylene glycol) helical foldamers. Synthesis, characterization, and complexation with ethane-1,2-diaminium. The Journal of organic chemistry, 69(19), 6228-37. https://doi.org/10.1021/jo049420n
Hou, Jun-Li, et al. "Solvophobically-driven oligo(ethylene glycol) helical foldamers. Synthesis, characterization, and complexation with ethane-1,2-diaminium." The Journal of organic chemistry vol. 69,19 (2004): 6228-37. doi: https://doi.org/10.1021/jo049420n
Hou JL, Jia MX, Jiang XK, Li ZT, Chen GJ. Solvophobically-driven oligo(ethylene glycol) helical foldamers. Synthesis, characterization, and complexation with ethane-1,2-diaminium. J Org Chem. 2004 Sep 17;69(19):6228-37. doi: 10.1021/jo049420n. PMID: 15357580.
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Showing 1 to 12 of 343 entries