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Ethyne functionalized meso-phenothiazinyl-phenyl-porphyrins: synthesis and optical properties of free base versus protonated species
- Source :
- Molecules, Molecules, Vol 25, Iss 4546, p 4546 (2020), Volume 25, Issue 19
- Publication Year :
- 2020
- Publisher :
- Zenodo, 2020.
-
Abstract
- Supplementary Materials: Figure S1. 1H-NMR spectrum of compound 2a, Figure S2. 13C-NMR spectrum of compound 2a, Figure S3. (1H-1H) COSY spectrum of compound 2a, Figure S4. (1H-13C) HMQC spectrum of compound 2a, Figure S5. 1H-NMR spectrum of compound 2b, Figure S6. 13C-NMR spectrum of compound 2b, Figure S7. 1H-NMR spectrum of compound 2e, Figure S8. 13C-NMR spectrum of compound 2e, Figure S9. 1H-NMR spectrum of compound 2f, Figure S10. 13C-NMR spectrum of compound 2f, Figure S11. (1H-1H) COSY spectrum of compound 2f, Figure S12. (1H-13C) HMQC spectrum of compound 2f, Figure S13. 1H-NMR spectrum of compound 2i, Figure S14. 13C-NMR spectrum of compound 2i, Figure S15. HRMS (APCI+) spectrum of compound 2b, Figure S16. HRMS (APCI+) spectrum of compound 2e, Figure S17. HRMS (APCI+) spectrum of compound 2f, Figure S18. HRMS (APCI+) spectrum of compound 2j.
- Subjects :
- Porphyrins
Absorption spectroscopy
phenothiazine
Pharmaceutical Science
Protonation
Photochemistry
Article
Analytical Chemistry
lcsh:QD241-441
chemistry.chemical_compound
lcsh:Organic chemistry
Drug Discovery
Bathochromic shift
Trifluoroacetic acid
Physical and Theoretical Chemistry
photophysical properties
Molecular Structure
Organic Chemistry
Free base
Porphyrin
Dication
chemistry
Chemistry (miscellaneous)
Molecular Medicine
Spectrophotometry, Ultraviolet
Hypsochromic shift
porphyrin derivatives
porphyrin
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Molecules, Molecules, Vol 25, Iss 4546, p 4546 (2020), Volume 25, Issue 19
- Accession number :
- edsair.doi.dedup.....cae595454e591243640973e9a30c394e
- Full Text :
- https://doi.org/10.5281/zenodo.4009582