Jewel Ann Maria Xavier
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Jewel Ann Maria Xavier has a total of 29 co-authors. Here are the top co-authors by number of shared publications:
- Clara Viñas
Institut de Ciència de Materials de Barcelona (ICMAB-CSIC), Campus UAB, 08193 Bellaterra, Spain
7 shared publications - Francesc Teixidor
Institut de Ciència de Materials de Barcelona (ICMAB-CSIC), Campus UAB, 08193 Bellaterra, Spain
7 shared publications Abdelazim M. A. Abdelgawwad
Departament de Química Física Universitat de València 46100 Burjassot Spain
2 shared publications- Antonio Francés-Monerris
Institut de Ciència Molecular Universitat de València València Spain
2 shared publications - Daniel Roca-Sanjuán
Universitat de València
2 shared publications - Isabel Fuentes
Institut de Ciència de Materials de Barcelona (ICMAB-CSIC), Campus de la UAB, Bellaterra, Spain
2 shared publications
Latest Publications
- Open Access
- 28 July 2023
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry B
- Vol. 11 (35) , 8422-8432
Single stop analysis of a protein surface using molecular probe electrochemistry
Two distinctive types of protein interactions modelled on the basis of basic amino acid residues on the protein surface using the anionic ‘small molecule’ probe [o-COSAN]−.
- 28 July 2023
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry B
- Vol. 11 (35) , 8422-8432
Open AccessSingle stop analysis of a protein surface using molecular probe electrochemistry
Two distinctive types of protein interactions modelled on the basis of basic amino acid residues on the protein surface using the anionic ‘small molecule’ probe [o-COSAN]−.
- Open Access
- 19 July 2022
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 10 (30) , 16182-16192
How to switch from a poor PEDOT:X oxygen evolution reaction (OER) to a good one. A study on dual redox reversible PEDOT:metallacarborane
Here, we dope an electroactive reversible redox polymer PEDOT with a reversible redox active metallacarborane having tunable potential to generate a synergistic material with superior properties such as a low overpotential to generate O 2 from water.
- 19 July 2022
- Published by Royal Society of Chemistry (RSC) in Journal of Materials Chemistry A
- Vol. 10 (30) , 16182-16192
Open AccessHow to switch from a poor PEDOT:X oxygen evolution reaction (OER) to a good one. A study on dual redox reversible PEDOT:metallacarborane
Here, we dope an electroactive reversible redox polymer PEDOT with a reversible redox active metallacarborane having tunable potential to generate a synergistic material with superior properties such as a low overpotential to generate O 2 from water.
- Open Access
- 6 April 2022
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 51 (18) , 7188-7209
Water soluble organometallic small molecules as promising antibacterial agents: synthesis, physical–chemical properties and biological evaluation to tackle bacterial infections
Small anionic metallacarborane molecules with activities down to the nanomolar range against methicillin resistant S. aureus (MRSA) and high selectivity index as promising antimicrobial agents to tackle antibiotic-resistant bacteria.
- 6 April 2022
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
- Vol. 51 (18) , 7188-7209
Open AccessWater soluble organometallic small molecules as promising antibacterial agents: synthesis, physical–chemical properties and biological evaluation to tackle bacterial infections
Small anionic metallacarborane molecules with activities down to the nanomolar range against methicillin resistant S. aureus (MRSA) and high selectivity index as promising antimicrobial agents to tackle antibiotic-resistant bacteria.
- Open Access
- 4 March 2022
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 58 (26) , 4196-4199
Potential application of metallacarboranes as an internal reference: an electrochemical comparative study to ferrocene
Ferrocene and its derivatives have been extensively used as an internal reference in electrochemical processes. Yet, they possess limitations such as solvent restrictions that require chemical modifications. In this regard, we have studied the use of metallacarboranes [3,3′-M(1,2-C2B9H11)2]− (M = Co, Fe) as general internal reference systems and have proven their suitability by thoroughly investigating their electrochemical properties in both aqueous and organic electrolytes without any derivatization.
- 4 March 2022
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 58 (26) , 4196-4199
Open AccessPotential application of metallacarboranes as an internal reference: an electrochemical comparative study to ferrocene
Ferrocene and its derivatives have been extensively used as an internal reference in electrochemical processes. Yet, they possess limitations such as solvent restrictions that require chemical modifications. In this regard, we have studied the use of metallacarboranes [3,3′-M(1,2-C2B9H11)2]− (M = Co, Fe) as general internal reference systems and have proven their suitability by thoroughly investigating their electrochemical properties in both aqueous and organic electrolytes without any derivatization.
- Open Access
Cobaltabis(dicarbollide) ([o-COSAN]−) as Multifunctional Chemotherapeutics: A Prospective Application in Boron Neutron Capture Therapy (BNCT) for Glioblastoma
Purpose: The aim of our study was to assess if the sodium salt of cobaltabis(dicarbollide) and its di-iodinated derivative (Na[o-COSAN] and Na[8,8′-I2-o-COSAN]) could be promising agents for dual anti-cancer treatment (chemotherapy + BNCT) for GBM. Methods: The biological activities of the small molecules were evaluated in vitro with glioblastoma cells lines U87 and T98G in 2D and 3D cell models and in vivo in the small model animal Caenorhabditis elegans (C. elegans) at the L4-stage and using the eggs. Results: Our studies indicated that only spheroids from the U87 cell line have impaired growth after treatment with both compounds, suggesting an increased resistance from T98G spheroids, contrary to what was observed in the monolayer culture, which highlights the need to employ 3D models for future GBM studies. In vitro tests in U87 and T98G cells conclude that the amount of 10B inside the cells is enough for BNCT irradiation. BNCT becomes more effective on T98G after their incubation with Na[8,8′-I2-o-COSAN], whereas no apparent cell-killing effect was observed for untreated cells. Conclusions: These small molecules, particularly [8,8′-I2-o-COSAN]−, are serious candidates for BNCT now that the facilities of accelerator-based neutron sources are more accessible, providing an alternative treatment for resistant glioblastoma.
Open AccessCobaltabis(dicarbollide) ([o-COSAN]−) as Multifunctional Chemotherapeutics: A Prospective Application in Boron Neutron Capture Therapy (BNCT) for Glioblastoma
Purpose: The aim of our study was to assess if the sodium salt of cobaltabis(dicarbollide) and its di-iodinated derivative (Na[o-COSAN] and Na[8,8′-I2-o-COSAN]) could be promising agents for dual anti-cancer treatment (chemotherapy + BNCT) for GBM. Methods: The biological activities of the small molecules were evaluated in vitro with glioblastoma cells lines U87 and T98G in 2D and 3D cell models and in vivo in the small model animal Caenorhabditis elegans (C. elegans) at the L4-stage and using the eggs. Results: Our studies indicated that only spheroids from the U87 cell line have impaired growth after treatment with both compounds, suggesting an increased resistance from T98G spheroids, contrary to what was observed in the monolayer culture, which highlights the need to employ 3D models for future GBM studies. In vitro tests in U87 and T98G cells conclude that the amount of 10B inside the cells is enough for BNCT irradiation. BNCT becomes more effective on T98G after their incubation with Na[8,8′-I2-o-COSAN], whereas no apparent cell-killing effect was observed for untreated cells. Conclusions: These small molecules, particularly [8,8′-I2-o-COSAN]−, are serious candidates for BNCT now that the facilities of accelerator-based neutron sources are more accessible, providing an alternative treatment for resistant glioblastoma.
- Open Access
- 25 September 2021
- Published by Wiley in Angewandte Chemie
- Vol. 133 (49) , 25957-25961
Light‐Induced On/Off Switching of the Surfactant Character of the o‐Cobaltabis(dicarbollide) Anion with No Covalent Bond Alteration
Cobaltabis(dicarbollide) anion ([o‐COSAN]−) is a well‐known metallacarborane with multiple applications in a variety of fields. In aqueous solution, the cisoid rotamer is the most stable disposition in the ground state. The present work provides theoretical evidence on the possibility to photoinduce the rotation from the cisoid to the transoid rotamer, a conversion that can be reverted when the ground state is repopulated. The non‐radiative decay mechanisms proposed in this work are coherent with the lack of fluorescence observed in 3D fluorescence mapping experiments performed on [o‐COSAN]− and its derivatives. This phenomenon induced by light has the potential to destruct the vesicles and micelles cisoid [o‐COSAN]− typically forms in aqueous solution, which could lead to promising applications, particularly in the field of nanomedicine.
- 25 September 2021
- Published by Wiley in Angewandte Chemie
- Vol. 133 (49) , 25957-25961
Open AccessLight‐Induced On/Off Switching of the Surfactant Character of the o‐Cobaltabis(dicarbollide) Anion with No Covalent Bond Alteration
Cobaltabis(dicarbollide) anion ([o‐COSAN]−) is a well‐known metallacarborane with multiple applications in a variety of fields. In aqueous solution, the cisoid rotamer is the most stable disposition in the ground state. The present work provides theoretical evidence on the possibility to photoinduce the rotation from the cisoid to the transoid rotamer, a conversion that can be reverted when the ground state is repopulated. The non‐radiative decay mechanisms proposed in this work are coherent with the lack of fluorescence observed in 3D fluorescence mapping experiments performed on [o‐COSAN]− and its derivatives. This phenomenon induced by light has the potential to destruct the vesicles and micelles cisoid [o‐COSAN]− typically forms in aqueous solution, which could lead to promising applications, particularly in the field of nanomedicine.
- Open Access
- 25 September 2021
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 60 (49) , 25753-25757
Light‐Induced On/Off Switching of the Surfactant Character of the o‐Cobaltabis(dicarbollide) Anion with No Covalent Bond Alteration
Cobaltabis(dicarbollide) anion ([o‐COSAN]−) is a well‐known metallacarborane with multiple applications in a variety of fields. In aqueous solution, the cisoid rotamer is the most stable disposition in the ground state. The present work provides theoretical evidence on the possibility to photoinduce the rotation from the cisoid to the transoid rotamer, a conversion that can be reverted when the ground state is repopulated. The non‐radiative decay mechanisms proposed in this work are coherent with the lack of fluorescence observed in 3D fluorescence mapping experiments performed on [o‐COSAN]− and its derivatives. This phenomenon induced by light has the potential to destruct the vesicles and micelles cisoid [o‐COSAN]− typically forms in aqueous solution, which could lead to promising applications, particularly in the field of nanomedicine.
- 25 September 2021
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 60 (49) , 25753-25757
Open AccessLight‐Induced On/Off Switching of the Surfactant Character of the o‐Cobaltabis(dicarbollide) Anion with No Covalent Bond Alteration
Cobaltabis(dicarbollide) anion ([o‐COSAN]−) is a well‐known metallacarborane with multiple applications in a variety of fields. In aqueous solution, the cisoid rotamer is the most stable disposition in the ground state. The present work provides theoretical evidence on the possibility to photoinduce the rotation from the cisoid to the transoid rotamer, a conversion that can be reverted when the ground state is repopulated. The non‐radiative decay mechanisms proposed in this work are coherent with the lack of fluorescence observed in 3D fluorescence mapping experiments performed on [o‐COSAN]− and its derivatives. This phenomenon induced by light has the potential to destruct the vesicles and micelles cisoid [o‐COSAN]− typically forms in aqueous solution, which could lead to promising applications, particularly in the field of nanomedicine.