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Highly Dynamic Ligand Binding and Light Absorption Coefficient of Cesium Lead Bromide Perovskite Nanocrystals.

ACS nano

De Roo J, Ibáñez M, Geiregat P, Nedelcu G, Walravens W, Maes J, Martins JC, Van Driessche I, Kovalenko MV, Hens Z.
PMID: 26786064
ACS Nano. 2016 Feb 23;10(2):2071-81. doi: 10.1021/acsnano.5b06295. Epub 2016 Jan 26.

Lead halide perovskite materials have attracted significant attention in the context of photovoltaics and other optoelectronic applications, and recently, research efforts have been directed to nanostructured lead halide perovskites. Collodial nanocrystals (NCs) of cesium lead halides (CsPbX3, X =...

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De Roo J, Ibáñez M, Geiregat P, et al. Highly Dynamic Ligand Binding and Light Absorption Coefficient of Cesium Lead Bromide Perovskite Nanocrystals. ACS Nano. 2016;10(2):2071-81doi: 10.1021/acsnano.5b06295.
De Roo, J., Ibáñez, M., Geiregat, P., Nedelcu, G., Walravens, W., Maes, J., Martins, J. C., Van Driessche, I., Kovalenko, M. V., & Hens, Z. (2016). Highly Dynamic Ligand Binding and Light Absorption Coefficient of Cesium Lead Bromide Perovskite Nanocrystals. ACS nano, 10(2), 2071-81. https://doi.org/10.1021/acsnano.5b06295
De Roo, Jonathan, et al. "Highly Dynamic Ligand Binding and Light Absorption Coefficient of Cesium Lead Bromide Perovskite Nanocrystals." ACS nano vol. 10,2 (2016): 2071-81. doi: https://doi.org/10.1021/acsnano.5b06295
De Roo J, Ibáñez M, Geiregat P, Nedelcu G, Walravens W, Maes J, Martins JC, Van Driessche I, Kovalenko MV, Hens Z. Highly Dynamic Ligand Binding and Light Absorption Coefficient of Cesium Lead Bromide Perovskite Nanocrystals. ACS Nano. 2016 Feb 23;10(2):2071-81. doi: 10.1021/acsnano.5b06295. Epub 2016 Jan 26. PMID: 26786064.
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Multifunctionalized sequence-defined oligomers from a single building block.

Angewandte Chemie (International ed. in English)

Espeel P, Carrette LL, Bury K, Capenberghs S, Martins JC, Du Prez FE, Madder A.
PMID: 24174322
Angew Chem Int Ed Engl. 2013 Dec 09;52(50):13261-4. doi: 10.1002/anie.201307439. Epub 2013 Oct 31.

No abstract available.

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Espeel P, Carrette LL, Bury K, et al. Multifunctionalized sequence-defined oligomers from a single building block. Angew Chem Int Ed Engl. 2013;52(50):13261-4doi: 10.1002/anie.201307439.
Espeel, P., Carrette, L. L., Bury, K., Capenberghs, S., Martins, J. C., Du Prez, F. E., & Madder, A. (2013). Multifunctionalized sequence-defined oligomers from a single building block. Angewandte Chemie (International ed. in English), 52(50), 13261-4. https://doi.org/10.1002/anie.201307439
Espeel, Pieter, et al. "Multifunctionalized sequence-defined oligomers from a single building block." Angewandte Chemie (International ed. in English) vol. 52,50 (2013): 13261-4. doi: https://doi.org/10.1002/anie.201307439
Espeel P, Carrette LL, Bury K, Capenberghs S, Martins JC, Du Prez FE, Madder A. Multifunctionalized sequence-defined oligomers from a single building block. Angew Chem Int Ed Engl. 2013 Dec 09;52(50):13261-4. doi: 10.1002/anie.201307439. Epub 2013 Oct 31. PMID: 24174322.
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Alkaline cations directing the transformation of FAU zeolites into five different framework types.

Chemical communications (Cambridge, England)

Van Tendeloo L, Gobechiya E, Breynaert E, Martens JA, Kirschhock CE.
PMID: 24202181
Chem Commun (Camb). 2013 Dec 28;49(100):11737-9. doi: 10.1039/c3cc47292b.

Exposure of faujasite zeolites to different alkali hydroxide solutions readily yields zeolites with ABW, CHA, MER and ANA topologies. In NaOH faujasite persisted. Aside from new opportunities for zeolite synthesis, this reveals that a suitable aluminosilicate connectivity in the...

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Van Tendeloo L, Gobechiya E, Breynaert E, et al. Alkaline cations directing the transformation of FAU zeolites into five different framework types. Chem Commun (Camb). 2013;49(100):11737-9doi: 10.1039/c3cc47292b.
Van Tendeloo, L., Gobechiya, E., Breynaert, E., Martens, J. A., & Kirschhock, C. E. (2013). Alkaline cations directing the transformation of FAU zeolites into five different framework types. Chemical communications (Cambridge, England), 49(100), 11737-9. https://doi.org/10.1039/c3cc47292b
Van Tendeloo, Leen, et al. "Alkaline cations directing the transformation of FAU zeolites into five different framework types." Chemical communications (Cambridge, England) vol. 49,100 (2013): 11737-9. doi: https://doi.org/10.1039/c3cc47292b
Van Tendeloo L, Gobechiya E, Breynaert E, Martens JA, Kirschhock CE. Alkaline cations directing the transformation of FAU zeolites into five different framework types. Chem Commun (Camb). 2013 Dec 28;49(100):11737-9. doi: 10.1039/c3cc47292b. PMID: 24202181.
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Nuclear Immunolocalization of Hexamerins in the Fat Body of Metamorphosing Honey Bees.

Insects

Martins JR, Bitondi MM.
PMID: 26466725
Insects. 2012 Oct 22;3(4):1039-55. doi: 10.3390/insects3041039.

Hexamerins are storage proteins with primordial functions in insect metamorphosis. They are actively secreted by the larval fat body and stored in the hemolymph. During metamorphosis, they return to the fat body to be processed. For decades, these proteins...

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Martins JR, Bitondi MM. Nuclear Immunolocalization of Hexamerins in the Fat Body of Metamorphosing Honey Bees. Insects. 2012;3(4):1039-55doi: 10.3390/insects3041039.
Martins, J. R., & Bitondi, M. M. (2012). Nuclear Immunolocalization of Hexamerins in the Fat Body of Metamorphosing Honey Bees. Insects, 3(4), 1039-55. https://doi.org/10.3390/insects3041039
Martins, Juliana Ramos, and Bitondi, Márcia Maria Gentile. "Nuclear Immunolocalization of Hexamerins in the Fat Body of Metamorphosing Honey Bees." Insects vol. 3,4 (2012): 1039-55. doi: https://doi.org/10.3390/insects3041039
Martins JR, Bitondi MM. Nuclear Immunolocalization of Hexamerins in the Fat Body of Metamorphosing Honey Bees. Insects. 2012 Oct 22;3(4):1039-55. doi: 10.3390/insects3041039. PMID: 26466725; PMCID: PMC4553562.
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Heterotopic ossification in breast prosthesis.

Eplasty

Fradinho N, Varanda A, Martins JB, Martins PA.
PMID: 25671058
Eplasty. 2015 Jan 23;15:ic7. eCollection 2015.

No abstract available.

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Fradinho N, Varanda A, Martins JB, et al. Heterotopic ossification in breast prosthesis. Eplasty. 2015;15:ic7
Fradinho, N., Varanda, A., Martins, J. B., & Martins, P. A. (2015). Heterotopic ossification in breast prosthesis. Eplasty, 15ic7.
Fradinho, Nuno, et al. "Heterotopic ossification in breast prosthesis." Eplasty vol. 15 (2015): ic7.
Fradinho N, Varanda A, Martins JB, Martins PA. Heterotopic ossification in breast prosthesis. Eplasty. 2015 Jan 23;15:ic7. eCollection 2015. PMID: 25671058; PMCID: PMC4313668.
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DeNOx of Exhaust Gas from Lean-Burn Engines through Reversible Adsorption of N(2)O(3) in Alkali Metal Cation Exchanged Faujasite-Type Zeolites This work was sponsored by the European Community (Brite Euram III projects BE-95-2127 "SNR Technique" and BE-97-4493 "SORPTEC") and the Belgium government (IUAP-PAI program).

Angewandte Chemie (International ed. in English)

Sultana A, Loenders R, Monticelli O, Kirschhock C, Jacobs PA, Martens JA.
PMID: 11028015
Angew Chem Int Ed Engl. 2000 Aug 18;39(16):2934-2937. doi: 10.1002/1521-3773(20000818)39:16<2934::aid-anie2934>3.0.co;2-e.

No abstract available.

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Sultana A, Loenders R, Monticelli O, et al. DeNOx of Exhaust Gas from Lean-Burn Engines through Reversible Adsorption of N(2)O(3) in Alkali Metal Cation Exchanged Faujasite-Type Zeolites This work was sponsored by the European Community (Brite Euram III projects BE-95-2127 "SNR Technique" and BE-97-4493 "SORPTEC") and the Belgium government (IUAP-PAI program). Angew Chem Int Ed Engl. 2000;39(16):2934-2937doi: 10.1002/1521-3773(20000818)39:16<2934::aid-anie2934>3.0.co;2-e.
Sultana, A., Loenders, R., Monticelli, O., Kirschhock, C., Jacobs, P. A., & Martens, J. A. (2000). DeNOx of Exhaust Gas from Lean-Burn Engines through Reversible Adsorption of N(2)O(3) in Alkali Metal Cation Exchanged Faujasite-Type Zeolites This work was sponsored by the European Community (Brite Euram III projects BE-95-2127 "SNR Technique" and BE-97-4493 "SORPTEC") and the Belgium government (IUAP-PAI program). Angewandte Chemie (International ed. in English), 39(16), 2934-2937. https://doi.org/10.1002/1521-3773(20000818)39:16<2934::aid-anie2934>3.0.co;2-e
Sultana, et al. "DeNOx of Exhaust Gas from Lean-Burn Engines through Reversible Adsorption of N(2)O(3) in Alkali Metal Cation Exchanged Faujasite-Type Zeolites This work was sponsored by the European Community (Brite Euram III projects BE-95-2127 "SNR Technique" and BE-97-4493 "SORPTEC") and the Belgium government (IUAP-PAI program)." Angewandte Chemie (International ed. in English) vol. 39,16 (2000): 2934-2937. doi: https://doi.org/10.1002/1521-3773(20000818)39:16<2934::aid-anie2934>3.0.co;2-e
Sultana A, Loenders R, Monticelli O, Kirschhock C, Jacobs PA, Martens JA. DeNOx of Exhaust Gas from Lean-Burn Engines through Reversible Adsorption of N(2)O(3) in Alkali Metal Cation Exchanged Faujasite-Type Zeolites This work was sponsored by the European Community (Brite Euram III projects BE-95-2127 "SNR Technique" and BE-97-4493 "SORPTEC") and the Belgium government (IUAP-PAI program). Angew Chem Int Ed Engl. 2000 Aug 18;39(16):2934-2937. doi: 10.1002/1521-3773(20000818)39:16<2934::aid-anie2934>3.0.co;2-e. PMID: 11028015.
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Transport of rimsulfuron and its metabolites in soil columns.

Chemosphere

Martins JM, Mermoud A.
PMID: 10901677
Chemosphere. 1999 Feb;38(3):601-16. doi: 10.1016/s0045-6535(98)00197-0.

This paper presents a study on degradation, sorption and transport of the sulfonylurea herbicide rimsulfuron and its major metabolites in alluvial soil columns. The formulation of rimsulfuron was found to strongly affect its degradability. Hydrolysis of pure rimsulfuron takes...

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Martins JM, Mermoud A. Transport of rimsulfuron and its metabolites in soil columns. Chemosphere. 1999;38(3):601-16doi: 10.1016/s0045-6535(98)00197-0.
Martins, J. M., & Mermoud, A. (1999). Transport of rimsulfuron and its metabolites in soil columns. Chemosphere, 38(3), 601-16. https://doi.org/10.1016/s0045-6535(98)00197-0
Martins, and Mermoud. "Transport of rimsulfuron and its metabolites in soil columns." Chemosphere vol. 38,3 (1999): 601-16. doi: https://doi.org/10.1016/s0045-6535(98)00197-0
Martins JM, Mermoud A. Transport of rimsulfuron and its metabolites in soil columns. Chemosphere. 1999 Feb;38(3):601-16. doi: 10.1016/s0045-6535(98)00197-0. PMID: 10901677.
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Complexation of triorganotin derivatives of [18]crown-6- and [15]crown-5-(benzo-4-carboxylate) with alkali thiocyanates.

Chemistry (Weinheim an der Bergstrasse, Germany)

Kemmer M, Biesemans M, Gielen M, Martins JC, Gramlich V, Willem R.
PMID: 11757661
Chemistry. 2001 Nov 05;7(21):4686-95. doi: 10.1002/1521-3765(20011105)7:21<4686::aid-chem4686>3.0.co;2-7.

Investigations of the simultaneous complexation of tri-n-butyltin and triphenyltin derivatives of [18]crown-6- or [15]crown-5-(benzo-4-carboxylate) by the anion and cation from NaSCN or KSCN are reported. The crystal structure of [Na+ is included in [15]crown-5-C6H3-4-COOSn(C6H5)3NCS]-], 4 NaSCN, displays an unusual...

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Kemmer M, Biesemans M, Gielen M, et al. Complexation of triorganotin derivatives of [18]crown-6- and [15]crown-5-(benzo-4-carboxylate) with alkali thiocyanates. Chemistry. 2001;7(21):4686-95doi: 10.1002/1521-3765(20011105)7:21<4686::aid-chem4686>3.0.co;2-7.
Kemmer, M., Biesemans, M., Gielen, M., Martins, J. C., Gramlich, V., & Willem, R. (2001). Complexation of triorganotin derivatives of [18]crown-6- and [15]crown-5-(benzo-4-carboxylate) with alkali thiocyanates. Chemistry (Weinheim an der Bergstrasse, Germany), 7(21), 4686-95. https://doi.org/10.1002/1521-3765(20011105)7:21<4686::aid-chem4686>3.0.co;2-7
Kemmer, M, et al. "Complexation of triorganotin derivatives of [18]crown-6- and [15]crown-5-(benzo-4-carboxylate) with alkali thiocyanates." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 7,21 (2001): 4686-95. doi: https://doi.org/10.1002/1521-3765(20011105)7:21<4686::aid-chem4686>3.0.co;2-7
Kemmer M, Biesemans M, Gielen M, Martins JC, Gramlich V, Willem R. Complexation of triorganotin derivatives of [18]crown-6- and [15]crown-5-(benzo-4-carboxylate) with alkali thiocyanates. Chemistry. 2001 Nov 05;7(21):4686-95. doi: 10.1002/1521-3765(20011105)7:21<4686::aid-chem4686>3.0.co;2-7. PMID: 11757661.
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Molecular competition effects in liquid-phase adsorption of long-chain n-alkane mixtures in ZSM-5 zeolite pores.

Angewandte Chemie (International ed. in English)

Denayer JF, De Meyer K, Martens JA, Baron GV.
PMID: 12820265
Angew Chem Int Ed Engl. 2003 Jun 23;42(24):2774-7. doi: 10.1002/anie.200351012.

No abstract available.

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Denayer JF, De Meyer K, Martens JA, et al. Molecular competition effects in liquid-phase adsorption of long-chain n-alkane mixtures in ZSM-5 zeolite pores. Angew Chem Int Ed Engl. 2003;42(24):2774-7doi: 10.1002/anie.200351012.
Denayer, J. F., De Meyer, K., Martens, J. A., & Baron, G. V. (2003). Molecular competition effects in liquid-phase adsorption of long-chain n-alkane mixtures in ZSM-5 zeolite pores. Angewandte Chemie (International ed. in English), 42(24), 2774-7. https://doi.org/10.1002/anie.200351012
Denayer, Joeri F M, et al. "Molecular competition effects in liquid-phase adsorption of long-chain n-alkane mixtures in ZSM-5 zeolite pores." Angewandte Chemie (International ed. in English) vol. 42,24 (2003): 2774-7. doi: https://doi.org/10.1002/anie.200351012
Denayer JF, De Meyer K, Martens JA, Baron GV. Molecular competition effects in liquid-phase adsorption of long-chain n-alkane mixtures in ZSM-5 zeolite pores. Angew Chem Int Ed Engl. 2003 Jun 23;42(24):2774-7. doi: 10.1002/anie.200351012. PMID: 12820265.
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Polystyrene-supported organotin dichloride as a recyclable catalyst in lactone ring-opening polymerization: assessment and catalysis monitoring by high-resolution magic-angle-spinning NMR spectroscopy.

Chemistry (Weinheim an der Bergstrasse, Germany)

Deshayes G, Poelmans K, Verbruggen I, Camacho-Camacho C, Degée P, Pinoie V, Martins JC, Piotto M, Biesemans M, Willem R, Dubois P.
PMID: 15900548
Chemistry. 2005 Jul 18;11(15):4552-61. doi: 10.1002/chem.200500065.

Dialkyltin dichloride grafted to a cross-linked polystyrene, with the formula [P-H]((1-t))[P-(CH2)nSnBuCl2]t (P=[CH2CH(pC6H4)], t=the degree of functionalization, and n=6 or 11), is investigated as a recyclable catalyst in the ring-opening polymerization (ROP) of epsilon-caprolactone (CL). It is demonstrated that high-resolution...

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Deshayes G, Poelmans K, Verbruggen I, et al. Polystyrene-supported organotin dichloride as a recyclable catalyst in lactone ring-opening polymerization: assessment and catalysis monitoring by high-resolution magic-angle-spinning NMR spectroscopy. Chemistry. 2005;11(15):4552-61doi: 10.1002/chem.200500065.
Deshayes, G., Poelmans, K., Verbruggen, I., Camacho-Camacho, C., Degée, P., Pinoie, V., Martins, J. C., Piotto, M., Biesemans, M., Willem, R., & Dubois, P. (2005). Polystyrene-supported organotin dichloride as a recyclable catalyst in lactone ring-opening polymerization: assessment and catalysis monitoring by high-resolution magic-angle-spinning NMR spectroscopy. Chemistry (Weinheim an der Bergstrasse, Germany), 11(15), 4552-61. https://doi.org/10.1002/chem.200500065
Deshayes, Gaëlle, et al. "Polystyrene-supported organotin dichloride as a recyclable catalyst in lactone ring-opening polymerization: assessment and catalysis monitoring by high-resolution magic-angle-spinning NMR spectroscopy." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 11,15 (2005): 4552-61. doi: https://doi.org/10.1002/chem.200500065
Deshayes G, Poelmans K, Verbruggen I, Camacho-Camacho C, Degée P, Pinoie V, Martins JC, Piotto M, Biesemans M, Willem R, Dubois P. Polystyrene-supported organotin dichloride as a recyclable catalyst in lactone ring-opening polymerization: assessment and catalysis monitoring by high-resolution magic-angle-spinning NMR spectroscopy. Chemistry. 2005 Jul 18;11(15):4552-61. doi: 10.1002/chem.200500065. PMID: 15900548.
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Electronic States of KxC60: Insulating, Metallic, and Superconducting Character.

Science (New York, N.Y.)

Benning PJ, Martins JL, Weaver JH, Chibante LP, Smalley RE.
PMID: 17772915
Science. 1991 Jun 07;252(5011):1417-9. doi: 10.1126/science.252.5011.1417.

The recent report of electrical conductivity in the alkali metal fullerides and the discovery of superconductivity at 18 K for KxC(60) has raised fundamental questions about the electronic states on either side of the Fermi level, their occupancy with...

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Benning PJ, Martins JL, Weaver JH, et al. Electronic States of KxC60: Insulating, Metallic, and Superconducting Character. Science. 1991;252(5011):1417-9doi: 10.1126/science.252.5011.1417.
Benning, P. J., Martins, J. L., Weaver, J. H., Chibante, L. P., & Smalley, R. E. (1991). Electronic States of KxC60: Insulating, Metallic, and Superconducting Character. Science (New York, N.Y.), 252(5011), 1417-9. https://doi.org/10.1126/science.252.5011.1417
Benning, P J, et al. "Electronic States of KxC60: Insulating, Metallic, and Superconducting Character." Science (New York, N.Y.) vol. 252,5011 (1991): 1417-9. doi: https://doi.org/10.1126/science.252.5011.1417
Benning PJ, Martins JL, Weaver JH, Chibante LP, Smalley RE. Electronic States of KxC60: Insulating, Metallic, and Superconducting Character. Science. 1991 Jun 07;252(5011):1417-9. doi: 10.1126/science.252.5011.1417. PMID: 17772915.
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In situ 1H NMR study on the trioctylphosphine oxide capping of colloidal InP nanocrystals.

Chemphyschem : a European journal of chemical physics and physical chemistry

Hens Z, Moreels I, Martins JC.
PMID: 16259026
Chemphyschem. 2005 Dec 09;6(12):2578-84. doi: 10.1002/cphc.200500182.

We used trioctylphosphine oxide (TOPO) capped colloidal InP nanocrystals (Q-InP|TOPO) to explore the potential of solution 1H NMR spectroscopy in studying in situ the capping and capping exchange of sterically stabilized colloidal nanocrystals. The spectrum of Q-InP|TOPO shows resonances...

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Hens Z, Moreels I, Martins JC. In situ 1H NMR study on the trioctylphosphine oxide capping of colloidal InP nanocrystals. Chemphyschem. 2005;6(12):2578-84doi: 10.1002/cphc.200500182.
Hens, Z., Moreels, I., & Martins, J. C. (2005). In situ 1H NMR study on the trioctylphosphine oxide capping of colloidal InP nanocrystals. Chemphyschem : a European journal of chemical physics and physical chemistry, 6(12), 2578-84. https://doi.org/10.1002/cphc.200500182
Hens, Zeger, et al. "In situ 1H NMR study on the trioctylphosphine oxide capping of colloidal InP nanocrystals." Chemphyschem : a European journal of chemical physics and physical chemistry vol. 6,12 (2005): 2578-84. doi: https://doi.org/10.1002/cphc.200500182
Hens Z, Moreels I, Martins JC. In situ 1H NMR study on the trioctylphosphine oxide capping of colloidal InP nanocrystals. Chemphyschem. 2005 Dec 09;6(12):2578-84. doi: 10.1002/cphc.200500182. PMID: 16259026.
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Showing 13 to 24 of 652 entries