A series of asymmetric and symmetric porphyrin derivatives: one-pot synthesis, nonlinear optical and optical limiting properties. (13th August 2021)
- Record Type:
- Journal Article
- Title:
- A series of asymmetric and symmetric porphyrin derivatives: one-pot synthesis, nonlinear optical and optical limiting properties. (13th August 2021)
- Main Title:
- A series of asymmetric and symmetric porphyrin derivatives: one-pot synthesis, nonlinear optical and optical limiting properties
- Authors:
- Bao, Changjiang
Li, Yanwei
Li, Yanhui
Si, Zhenjun
Zhang, Yanru
Chen, Changshun
Wang, Lei
Duan, Qian - Abstract:
- Abstract : In this work, a series of asymmetric and symmetric porphyrin derivatives (structure types: A4, A3 B1, trans -A2 B2, cis -A2 B2, A1 B3, and B4 ) have been synthesized via a one-pot method and characterized to identify their structures and properties. Abstract : In this work, a series of asymmetric and symmetric porphyrin derivatives (structure types: A4, A3 B1, trans -A2 B2, cis -A2 B2, A1 B3, and B4 ) have been synthesized via a one-pot method and characterized by TLC, HPLC, FT-IR, 1 H-NMR and UV-Vis to identify their structures and properties. The porphyrin derivatives with trans -A2 B2 and cis -A2 B2 structures are visually distinguished via single-crystal X-ray diffraction; the crystal morphology of trans -A2 B2 is a needle-like structure. All porphyrin derivatives (I–VI ) have excellent nonlinear optical (NLO) and optical limiting (OL) properties, and are investigated using the standard Z -scan technique. Porphyrin derivative III exhibits the maximum nonlinear absorption, nonlinear refraction coefficients and optical limitation threshold, and the values are 3.7 × 10 −9 m W −1, −17 × 10 −17 m 2 W −1 and 0.11 J cm −2, respectively. The results demonstrate that the introduction of different substituent numbers (mono-, di- and tri-, tetra-) and substituent sites ( trans -A2 B2 and cis -A2 B2 ) in the porphyrins could influence the NLO and OL properties. Structure regulation of porphyrin can lead to the adjustment of NLO and OL properties, and affect its practicalAbstract : In this work, a series of asymmetric and symmetric porphyrin derivatives (structure types: A4, A3 B1, trans -A2 B2, cis -A2 B2, A1 B3, and B4 ) have been synthesized via a one-pot method and characterized to identify their structures and properties. Abstract : In this work, a series of asymmetric and symmetric porphyrin derivatives (structure types: A4, A3 B1, trans -A2 B2, cis -A2 B2, A1 B3, and B4 ) have been synthesized via a one-pot method and characterized by TLC, HPLC, FT-IR, 1 H-NMR and UV-Vis to identify their structures and properties. The porphyrin derivatives with trans -A2 B2 and cis -A2 B2 structures are visually distinguished via single-crystal X-ray diffraction; the crystal morphology of trans -A2 B2 is a needle-like structure. All porphyrin derivatives (I–VI ) have excellent nonlinear optical (NLO) and optical limiting (OL) properties, and are investigated using the standard Z -scan technique. Porphyrin derivative III exhibits the maximum nonlinear absorption, nonlinear refraction coefficients and optical limitation threshold, and the values are 3.7 × 10 −9 m W −1, −17 × 10 −17 m 2 W −1 and 0.11 J cm −2, respectively. The results demonstrate that the introduction of different substituent numbers (mono-, di- and tri-, tetra-) and substituent sites ( trans -A2 B2 and cis -A2 B2 ) in the porphyrins could influence the NLO and OL properties. Structure regulation of porphyrin can lead to the adjustment of NLO and OL properties, and affect its practical NLO application in the future. … (more)
- Is Part Of:
- New journal of chemistry. Volume 45:Number 35(2021)
- Journal:
- New journal of chemistry
- Issue:
- Volume 45:Number 35(2021)
- Issue Display:
- Volume 45, Issue 35 (2021)
- Year:
- 2021
- Volume:
- 45
- Issue:
- 35
- Issue Sort Value:
- 2021-0045-0035-0000
- Page Start:
- 16030
- Page End:
- 16038
- Publication Date:
- 2021-08-13
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d1nj02632a ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21718.xml