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Bifunctional Indenyl-Derived Receptors for Fluoride Chelation and Detection.

Chemistry (Weinheim an der Bergstrasse, Germany)

Tirfoin R, Abdalla JA, Aldridge S.
PMID: 26179477
Chemistry. 2015 Aug 10;21(33):11813-24. doi: 10.1002/chem.201501547. Epub 2015 Jul 15.

Anion receptors based on a [CpFe(indenyl)] scaffold offer the possibility for the incorporation of adjacent Lewis acidic functions onto a six-membered carbocyclic framework, while at the same time retaining the colorimetric/electrochemical reporter mechanisms available to synthetically simpler ferrocene systems....

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Tirfoin R, Abdalla JA, Aldridge S. Bifunctional Indenyl-Derived Receptors for Fluoride Chelation and Detection. Chemistry. 2015;21(33):11813-24doi: 10.1002/chem.201501547.
Tirfoin, R., Abdalla, J. A., & Aldridge, S. (2015). Bifunctional Indenyl-Derived Receptors for Fluoride Chelation and Detection. Chemistry (Weinheim an der Bergstrasse, Germany), 21(33), 11813-24. https://doi.org/10.1002/chem.201501547
Tirfoin, Rémi, et al. "Bifunctional Indenyl-Derived Receptors for Fluoride Chelation and Detection." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,33 (2015): 11813-24. doi: https://doi.org/10.1002/chem.201501547
Tirfoin R, Abdalla JA, Aldridge S. Bifunctional Indenyl-Derived Receptors for Fluoride Chelation and Detection. Chemistry. 2015 Aug 10;21(33):11813-24. doi: 10.1002/chem.201501547. Epub 2015 Jul 15. PMID: 26179477.
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Synthesis, characterization, and cytotoxicity in human erythrocytes of multifunctional, magnetic, and luminescent nanocrystalline rare earth fluorides.

Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology

Grzyb T, Mrówczyńska L, Szczeszak A, Śniadecki Z, Runowski M, Idzikowski B, Lis S.
PMID: 26457061
J Nanopart Res. 2015;17(10):399. doi: 10.1007/s11051-015-3191-2. Epub 2015 Oct 05.

Multifunctional nanoparticles exhibiting red or green luminescence properties and magnetism were synthesized and thoroughly analyzed. The hydrothermal method was used for the synthesis of Eu

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Grzyb T, Mrówczyńska L, Szczeszak A, et al. Synthesis, characterization, and cytotoxicity in human erythrocytes of multifunctional, magnetic, and luminescent nanocrystalline rare earth fluorides. J Nanopart Res. 2015;17(10):399doi: 10.1007/s11051-015-3191-2.
Grzyb, T., Mrówczyńska, L., Szczeszak, A., Śniadecki, Z., Runowski, M., Idzikowski, B., & Lis, S. (2015). Synthesis, characterization, and cytotoxicity in human erythrocytes of multifunctional, magnetic, and luminescent nanocrystalline rare earth fluorides. Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology, 17(10), 399. https://doi.org/10.1007/s11051-015-3191-2
Grzyb, Tomasz, et al. "Synthesis, characterization, and cytotoxicity in human erythrocytes of multifunctional, magnetic, and luminescent nanocrystalline rare earth fluorides." Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology vol. 17,10 (2015): 399. doi: https://doi.org/10.1007/s11051-015-3191-2
Grzyb T, Mrówczyńska L, Szczeszak A, Śniadecki Z, Runowski M, Idzikowski B, Lis S. Synthesis, characterization, and cytotoxicity in human erythrocytes of multifunctional, magnetic, and luminescent nanocrystalline rare earth fluorides. J Nanopart Res. 2015;17(10):399. doi: 10.1007/s11051-015-3191-2. Epub 2015 Oct 05. PMID: 26457061; PMCID: PMC4594090.
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Crystal Structures of Diaryliodonium Fluorides and Their Implications for Fluorination Mechanisms.

Chemistry (Weinheim an der Bergstrasse, Germany)

Lee YS, Chun JH, Hodošček M, Pike VW.
PMID: 28145069
Chemistry. 2017 Mar 28;23(18):4353-4363. doi: 10.1002/chem.201604803. Epub 2017 Mar 02.

The radiofluorination of diaryliodonium salts is of value for producing radiotracers for positron emission tomography. We report crystal structures for two diaryliodonium fluorides. Whereas diphenyliodonium fluoride (1 a) exists as a tetramer bridged by four fluoride ions, 2-methylphenyl(phenyl)iodonium fluoride...

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Lee YS, Chun JH, Hodošček M, et al. Crystal Structures of Diaryliodonium Fluorides and Their Implications for Fluorination Mechanisms. Chemistry. 2017;23(18):4353-4363doi: 10.1002/chem.201604803.
Lee, Y. S., Chun, J. H., Hodošček, M., & Pike, V. W. (2017). Crystal Structures of Diaryliodonium Fluorides and Their Implications for Fluorination Mechanisms. Chemistry (Weinheim an der Bergstrasse, Germany), 23(18), 4353-4363. https://doi.org/10.1002/chem.201604803
Lee, Yong-Sok, et al. "Crystal Structures of Diaryliodonium Fluorides and Their Implications for Fluorination Mechanisms." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 23,18 (2017): 4353-4363. doi: https://doi.org/10.1002/chem.201604803
Lee YS, Chun JH, Hodošček M, Pike VW. Crystal Structures of Diaryliodonium Fluorides and Their Implications for Fluorination Mechanisms. Chemistry. 2017 Mar 28;23(18):4353-4363. doi: 10.1002/chem.201604803. Epub 2017 Mar 02. PMID: 28145069; PMCID: PMC5687088.
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Carbene complexes of phosphorus(V) fluorides substituted with perfluoroalkyl-groups synthesized by oxidative addition. Cleavage of the complexes reveals a new synthetic protocol for ionic liquids.

Dalton transactions (Cambridge, England : 2003)

Böttcher T, Steinhauer S, Allefeld N, Hoge B, Neumann B, Stammler HG, Bassil BS, Winter M, Mitzel NW, Röschenthaler GV.
PMID: 24346352
Dalton Trans. 2014 Feb 21;43(7):2979-87. doi: 10.1039/c3dt53043d.

The crystal structures of the previously reported 2,2-difluoro-1,3-dimethylimidazolidine and its acyclic analog were determined by in situ crystallization. Both liquid fluorinating agents have recently been introduced as potent precursors for the synthesis of p-block element carbene complexes. These fluorine...

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Böttcher T, Steinhauer S, Allefeld N, et al. Carbene complexes of phosphorus(V) fluorides substituted with perfluoroalkyl-groups synthesized by oxidative addition. Cleavage of the complexes reveals a new synthetic protocol for ionic liquids. Dalton Trans. 2014;43(7):2979-87doi: 10.1039/c3dt53043d.
Böttcher, T., Steinhauer, S., Allefeld, N., Hoge, B., Neumann, B., Stammler, H. G., Bassil, B. S., Winter, M., Mitzel, N. W., & Röschenthaler, G. V. (2014). Carbene complexes of phosphorus(V) fluorides substituted with perfluoroalkyl-groups synthesized by oxidative addition. Cleavage of the complexes reveals a new synthetic protocol for ionic liquids. Dalton transactions (Cambridge, England : 2003), 43(7), 2979-87. https://doi.org/10.1039/c3dt53043d
Böttcher, Tobias, et al. "Carbene complexes of phosphorus(V) fluorides substituted with perfluoroalkyl-groups synthesized by oxidative addition. Cleavage of the complexes reveals a new synthetic protocol for ionic liquids." Dalton transactions (Cambridge, England : 2003) vol. 43,7 (2014): 2979-87. doi: https://doi.org/10.1039/c3dt53043d
Böttcher T, Steinhauer S, Allefeld N, Hoge B, Neumann B, Stammler HG, Bassil BS, Winter M, Mitzel NW, Röschenthaler GV. Carbene complexes of phosphorus(V) fluorides substituted with perfluoroalkyl-groups synthesized by oxidative addition. Cleavage of the complexes reveals a new synthetic protocol for ionic liquids. Dalton Trans. 2014 Feb 21;43(7):2979-87. doi: 10.1039/c3dt53043d. PMID: 24346352.
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High-pressure stabilization of argon fluorides.

Physical chemistry chemical physics : PCCP

Kurzydłowski D, Zaleski-Ejgierd P.
PMID: 26742478
Phys Chem Chem Phys. 2016 Jan 28;18(4):2309-13. doi: 10.1039/c5cp05725f.

On account of the rapid development of noble gas chemistry in the past half-century both xenon and krypton compounds can now be isolated in macroscopic quantities. The same does not hold true for the next lighter group 18 element,...

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Kurzydłowski D, Zaleski-Ejgierd P. High-pressure stabilization of argon fluorides. Phys Chem Chem Phys. 2016;18(4):2309-13doi: 10.1039/c5cp05725f.
Kurzydłowski, D., & Zaleski-Ejgierd, P. (2016). High-pressure stabilization of argon fluorides. Physical chemistry chemical physics : PCCP, 18(4), 2309-13. https://doi.org/10.1039/c5cp05725f
Kurzydłowski, Dominik, and Zaleski-Ejgierd, Patryk. "High-pressure stabilization of argon fluorides." Physical chemistry chemical physics : PCCP vol. 18,4 (2016): 2309-13. doi: https://doi.org/10.1039/c5cp05725f
Kurzydłowski D, Zaleski-Ejgierd P. High-pressure stabilization of argon fluorides. Phys Chem Chem Phys. 2016 Jan 28;18(4):2309-13. doi: 10.1039/c5cp05725f. PMID: 26742478.
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CO2 Conversion into Esters by Fluoride-Mediated Carboxylation of Organosilanes and Halide Derivatives.

Chemistry (Weinheim an der Bergstrasse, Germany)

Frogneux X, von Wolff N, Thuéry P, Lefèvre G, Cantat T.
PMID: 26712565
Chemistry. 2016 Feb 24;22(9):2930-4. doi: 10.1002/chem.201505092. Epub 2016 Jan 25.

A one-step conversion of CO2 into heteroaromatic esters is presented under metal-free conditions. Using fluoride anions as promoters for the C-Si bond activation, pyridyl, furanyl, and thienyl organosilanes are successfully carboxylated with CO2 in the presence of an electrophile....

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Frogneux X, von Wolff N, Thuéry P, et al. CO2 Conversion into Esters by Fluoride-Mediated Carboxylation of Organosilanes and Halide Derivatives. Chemistry. 2016;22(9):2930-4doi: 10.1002/chem.201505092.
Frogneux, X., von Wolff, N., Thuéry, P., Lefèvre, G., & Cantat, T. (2016). CO2 Conversion into Esters by Fluoride-Mediated Carboxylation of Organosilanes and Halide Derivatives. Chemistry (Weinheim an der Bergstrasse, Germany), 22(9), 2930-4. https://doi.org/10.1002/chem.201505092
Frogneux, Xavier, et al. "CO2 Conversion into Esters by Fluoride-Mediated Carboxylation of Organosilanes and Halide Derivatives." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,9 (2016): 2930-4. doi: https://doi.org/10.1002/chem.201505092
Frogneux X, von Wolff N, Thuéry P, Lefèvre G, Cantat T. CO2 Conversion into Esters by Fluoride-Mediated Carboxylation of Organosilanes and Halide Derivatives. Chemistry. 2016 Feb 24;22(9):2930-4. doi: 10.1002/chem.201505092. Epub 2016 Jan 25. PMID: 26712565.
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The effect of different fluoride application methods on the remineralization of initial carious lesions.

Restorative dentistry & endodontics

Byeon SM, Lee MH, Bae TS.
PMID: 27200280
Restor Dent Endod. 2016 May;41(2):121-9. doi: 10.5395/rde.2016.41.2.121. Epub 2016 May 10.

OBJECTIVES: The purpose of this study was to assess the effect of single and combined applications of fluoride on the amount of fluoride release, and the remineralization and physical properties of enamel.MATERIALS AND METHODS: Each of four fluoride varnish...

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Byeon SM, Lee MH, Bae TS. The effect of different fluoride application methods on the remineralization of initial carious lesions. Restor Dent Endod. 2016;41(2):121-9doi: 10.5395/rde.2016.41.2.121.
Byeon, S. M., Lee, M. H., & Bae, T. S. (2016). The effect of different fluoride application methods on the remineralization of initial carious lesions. Restorative dentistry & endodontics, 41(2), 121-9. https://doi.org/10.5395/rde.2016.41.2.121
Byeon, Seon Mi, et al. "The effect of different fluoride application methods on the remineralization of initial carious lesions." Restorative dentistry & endodontics vol. 41,2 (2016): 121-9. doi: https://doi.org/10.5395/rde.2016.41.2.121
Byeon SM, Lee MH, Bae TS. The effect of different fluoride application methods on the remineralization of initial carious lesions. Restor Dent Endod. 2016 May;41(2):121-9. doi: 10.5395/rde.2016.41.2.121. Epub 2016 May 10. PMID: 27200280; PMCID: PMC4868875.
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A Comparative Evaluation of the Amount of Fluoride Release and Re-Release after Recharging from Aesthetic Restorative Materials: An in vitro Study.

Journal of clinical and diagnostic research : JCDR

Bansal R, Bansal T.
PMID: 26436037
J Clin Diagn Res. 2015 Aug;9(8):ZC11-4. doi: 10.7860/JCDR/2015/11926.6278. Epub 2015 Aug 01.

AIM: To measure the amount of fluoride released and re released after recharging from various restorative materials: Conventional Glass Ionomer Cement (Fuji II), Light Cure Resin Modified GIC (Fuji II LC), Giomer (Beautifil II), Compomer (Dyract).MATERIALS AND METHODS: Fifteen...

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Bansal R, Bansal T. A Comparative Evaluation of the Amount of Fluoride Release and Re-Release after Recharging from Aesthetic Restorative Materials: An in vitro Study. J Clin Diagn Res. 2015;9(8):ZC11-4doi: 10.7860/JCDR/2015/11926.6278.
Bansal, R., & Bansal, T. (2015). A Comparative Evaluation of the Amount of Fluoride Release and Re-Release after Recharging from Aesthetic Restorative Materials: An in vitro Study. Journal of clinical and diagnostic research : JCDR, 9(8), ZC11-4. https://doi.org/10.7860/JCDR/2015/11926.6278
Bansal, Ruchika, and Bansal, Tajinder. "A Comparative Evaluation of the Amount of Fluoride Release and Re-Release after Recharging from Aesthetic Restorative Materials: An in vitro Study." Journal of clinical and diagnostic research : JCDR vol. 9,8 (2015): ZC11-4. doi: https://doi.org/10.7860/JCDR/2015/11926.6278
Bansal R, Bansal T. A Comparative Evaluation of the Amount of Fluoride Release and Re-Release after Recharging from Aesthetic Restorative Materials: An in vitro Study. J Clin Diagn Res. 2015 Aug;9(8):ZC11-4. doi: 10.7860/JCDR/2015/11926.6278. Epub 2015 Aug 01. PMID: 26436037; PMCID: PMC4576631.
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Rhodium-catalyzed transformation of heteroaryl aryl ethers into heteroaryl fluorides.

Chemical communications (Cambridge, England)

Arisawa M, Tanii S, Tazawa T, Yamaguchi M.
PMID: 27709178
Chem Commun (Camb). 2016 Sep 15;52(76):11390-11393. doi: 10.1039/c6cc05400e.

A rhodium complex catalyzed the conversion of the C-O bond of heteroaryl aryl ethers to the C-F bond. The reaction of (4-chlorophenylthio)pentafluorobenzene with heteroaryl aryl ethers provided heteroaryl fluorides and heteroaryl (4-chlorophenylthio)tetrafluorophenyl ethers; this involved the cleavage of a...

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Arisawa M, Tanii S, Tazawa T, et al. Rhodium-catalyzed transformation of heteroaryl aryl ethers into heteroaryl fluorides. Chem Commun (Camb). 2016;52(76):11390-11393doi: 10.1039/c6cc05400e.
Arisawa, M., Tanii, S., Tazawa, T., & Yamaguchi, M. (2016). Rhodium-catalyzed transformation of heteroaryl aryl ethers into heteroaryl fluorides. Chemical communications (Cambridge, England), 52(76), 11390-11393. https://doi.org/10.1039/c6cc05400e
Arisawa, Mieko, et al. "Rhodium-catalyzed transformation of heteroaryl aryl ethers into heteroaryl fluorides." Chemical communications (Cambridge, England) vol. 52,76 (2016): 11390-11393. doi: https://doi.org/10.1039/c6cc05400e
Arisawa M, Tanii S, Tazawa T, Yamaguchi M. Rhodium-catalyzed transformation of heteroaryl aryl ethers into heteroaryl fluorides. Chem Commun (Camb). 2016 Sep 15;52(76):11390-11393. doi: 10.1039/c6cc05400e. PMID: 27709178.
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Direct Synthesis of Acyl Fluorides from Carboxylic Acids with the Bench-Stable Solid Reagent (Me.

Organic letters

Scattolin T, Deckers K, Schoenebeck F.
PMID: 29023131
Org Lett. 2017 Nov 03;19(21):5740-5743. doi: 10.1021/acs.orglett.7b02516.

A convenient, highly efficient, and selective transformation of aliphatic and aromatic carboxylic acids to acyl fluorides is reported. In contrast to established approaches that require toxic or volatile additives and base and reaction control (i.e., cooling, slow addition), this...

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Scattolin T, Deckers K, Schoenebeck F. Direct Synthesis of Acyl Fluorides from Carboxylic Acids with the Bench-Stable Solid Reagent (Me. Org Lett. 2017;19(21):5740-5743doi: 10.1021/acs.orglett.7b02516.
Scattolin, T., Deckers, K., & Schoenebeck, F. (2017). Direct Synthesis of Acyl Fluorides from Carboxylic Acids with the Bench-Stable Solid Reagent (Me. Organic letters, 19(21), 5740-5743. https://doi.org/10.1021/acs.orglett.7b02516
Scattolin, Thomas, et al. "Direct Synthesis of Acyl Fluorides from Carboxylic Acids with the Bench-Stable Solid Reagent (Me." Organic letters vol. 19,21 (2017): 5740-5743. doi: https://doi.org/10.1021/acs.orglett.7b02516
Scattolin T, Deckers K, Schoenebeck F. Direct Synthesis of Acyl Fluorides from Carboxylic Acids with the Bench-Stable Solid Reagent (Me. Org Lett. 2017 Nov 03;19(21):5740-5743. doi: 10.1021/acs.orglett.7b02516. PMID: 29023131.
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Titanium Ions Release from an Innovative Titanium-Magnesium Composite: an in Vitro Study.

Acta stomatologica Croatica

Stanec Z, Halambek J, Maldini K, Balog M, Križik P, Schauperl Z, Ćatić A.
PMID: 27688425
Acta Stomatol Croat. 2016 Mar;50(1):40-8. doi: 10.15644/asc50/1/6.

BACKGROUND: The innovative titanium-magnesium composite (Ti-Mg) was produced by powder metallurgy (P/M) method and is characterized in terms of corrosion behavior.MATERIAL AND METHODS: Two groups of experimental material, 1 mass% (Ti-1Mg) and 2 mass% (Ti-2Mg) of magnesium in titanium...

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Stanec Z, Halambek J, Maldini K, et al. Titanium Ions Release from an Innovative Titanium-Magnesium Composite: an in Vitro Study. Acta Stomatol Croat. 2016;50(1):40-8doi: 10.15644/asc50/1/6.
Stanec, Z., Halambek, J., Maldini, K., Balog, M., Križik, P., Schauperl, Z., & Ćatić, A. (2016). Titanium Ions Release from an Innovative Titanium-Magnesium Composite: an in Vitro Study. Acta stomatologica Croatica, 50(1), 40-8. https://doi.org/10.15644/asc50/1/6
Stanec, Zlatko, et al. "Titanium Ions Release from an Innovative Titanium-Magnesium Composite: an in Vitro Study." Acta stomatologica Croatica vol. 50,1 (2016): 40-8. doi: https://doi.org/10.15644/asc50/1/6
Stanec Z, Halambek J, Maldini K, Balog M, Križik P, Schauperl Z, Ćatić A. Titanium Ions Release from an Innovative Titanium-Magnesium Composite: an in Vitro Study. Acta Stomatol Croat. 2016 Mar;50(1):40-8. doi: 10.15644/asc50/1/6. PMID: 27688425; PMCID: PMC5017277.
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First-Principles Analysis of Defect Thermodynamics and Ion Transport in Inorganic SEI Compounds: LiF and NaF.

ACS applied materials & interfaces

Yildirim H, Kinaci A, Chan MK, Greeley JP.
PMID: 26255641
ACS Appl Mater Interfaces. 2015 Sep 02;7(34):18985-96. doi: 10.1021/acsami.5b02904. Epub 2015 Aug 24.

The formation mechanism and composition of the solid electrolyte interphase (SEI) in lithium ion batteries has been widely explored. However, relatively little is known about the function of the SEI as a transport medium. Such critical information is directly...

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Yildirim H, Kinaci A, Chan MK, et al. First-Principles Analysis of Defect Thermodynamics and Ion Transport in Inorganic SEI Compounds: LiF and NaF. ACS Appl Mater Interfaces. 2015;7(34):18985-96doi: 10.1021/acsami.5b02904.
Yildirim, H., Kinaci, A., Chan, M. K., & Greeley, J. P. (2015). First-Principles Analysis of Defect Thermodynamics and Ion Transport in Inorganic SEI Compounds: LiF and NaF. ACS applied materials & interfaces, 7(34), 18985-96. https://doi.org/10.1021/acsami.5b02904
Yildirim, Handan, et al. "First-Principles Analysis of Defect Thermodynamics and Ion Transport in Inorganic SEI Compounds: LiF and NaF." ACS applied materials & interfaces vol. 7,34 (2015): 18985-96. doi: https://doi.org/10.1021/acsami.5b02904
Yildirim H, Kinaci A, Chan MK, Greeley JP. First-Principles Analysis of Defect Thermodynamics and Ion Transport in Inorganic SEI Compounds: LiF and NaF. ACS Appl Mater Interfaces. 2015 Sep 02;7(34):18985-96. doi: 10.1021/acsami.5b02904. Epub 2015 Aug 24. PMID: 26255641.
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Showing 13 to 24 of 1102 entries