S,S-Chiral Linker Induced U Shape with a Syn-facial Sensitizer and Photocleavable Ethene Group
There is a major need for light-activated materials for the release of sensitizers and drugs. Considering the success of chiral columns for the separation of enantiomer drugs, we synthesized an S,S-chiral linker system covalently attached to silica with a sensitizer ethene near the silica surface....
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| Autores principales: | , , , , , , , , , |
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| Formato: | Articulo Preprint |
| Lenguaje: | Inglés |
| Publicado: |
2019
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| Materias: | |
| Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/107002 http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC6347524&blobtype=pdf |
| Aporte de: |
| id |
I19-R120-10915-107002 |
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| record_format |
dspace |
| institution |
Universidad Nacional de La Plata |
| institution_str |
I-19 |
| repository_str |
R-120 |
| collection |
SEDICI (UNLP) |
| language |
Inglés |
| topic |
Química S,S-chiral linker system Drug photorelease |
| spellingShingle |
Química S,S-chiral linker system Drug photorelease Ghosh, Goutam Belh, Sarah J. Chiemezie, Callistus Walalawela, Niluksha Ghogare, Ashwini A. Vignoni, Mariana Thomas, Andrés Héctor McFarland, Sherri A. Greer, Edyta M. Greer, Alexander S,S-Chiral Linker Induced U Shape with a Syn-facial Sensitizer and Photocleavable Ethene Group |
| topic_facet |
Química S,S-chiral linker system Drug photorelease |
| description |
There is a major need for light-activated materials for the release of sensitizers and drugs.
Considering the success of chiral columns for the separation of enantiomer drugs, we synthesized an S,S-chiral linker system covalently attached to silica with a sensitizer ethene near the silica surface. First, the silica surface was modified to be aromatic rich, by replacing 70% of the surface groups with (3-phenoxypropyl)silane. We then synthesized a 3-component conjugate [chlorin sensitizer, S,S-chiral cyclohexane, and ethene building blocks] in 5 steps with a 13% yield, and covalently bound the conjugate to the (3-phenoxypropyl)silane-coated silica surface. We hypothesized that the chiral linker would increase exposure of the ethene site for enhanced 1O2- based sensitizer release. However, the chiral linker caused the sensitizer conjugate to adopt a Ushape due to favored 1,2-diaxial substituent orientation; resulting in a reduced efficiency of surface loading. Further accentuating the U-shape was π–π stacking between the (3-phenoxypropyl)silane and sensitizer. Semiempirical calculations and singlet oxygen luminescence data provided deeper insight into the sensitizer’s orientation and release. This study has lead to insight on modifications of surfaces for drug photorelease and can help lead to the development of miniaturized photodynamic devices. |
| format |
Articulo Preprint |
| author |
Ghosh, Goutam Belh, Sarah J. Chiemezie, Callistus Walalawela, Niluksha Ghogare, Ashwini A. Vignoni, Mariana Thomas, Andrés Héctor McFarland, Sherri A. Greer, Edyta M. Greer, Alexander |
| author_facet |
Ghosh, Goutam Belh, Sarah J. Chiemezie, Callistus Walalawela, Niluksha Ghogare, Ashwini A. Vignoni, Mariana Thomas, Andrés Héctor McFarland, Sherri A. Greer, Edyta M. Greer, Alexander |
| author_sort |
Ghosh, Goutam |
| title |
S,S-Chiral Linker Induced U Shape with a Syn-facial Sensitizer and Photocleavable Ethene Group |
| title_short |
S,S-Chiral Linker Induced U Shape with a Syn-facial Sensitizer and Photocleavable Ethene Group |
| title_full |
S,S-Chiral Linker Induced U Shape with a Syn-facial Sensitizer and Photocleavable Ethene Group |
| title_fullStr |
S,S-Chiral Linker Induced U Shape with a Syn-facial Sensitizer and Photocleavable Ethene Group |
| title_full_unstemmed |
S,S-Chiral Linker Induced U Shape with a Syn-facial Sensitizer and Photocleavable Ethene Group |
| title_sort |
s,s-chiral linker induced u shape with a syn-facial sensitizer and photocleavable ethene group |
| publishDate |
2019 |
| url |
http://sedici.unlp.edu.ar/handle/10915/107002 http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC6347524&blobtype=pdf |
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Repositorios |
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