SUPPLEMENTARY MATERIAL Synthesis, photophysical and ...

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10.1071/CH17652_AC

CSIRO 2018

Australian Journal of Chemistry 2018, 71(6), 399-406

SUPPLEMENTARY MATERIAL

Synthesis, photophysical and antioxidant properties of rhodamine B

decorated novel dendrimers

Jothinathan Sathiya Savithri and Perumal Rajakumar*

Department of Organic Chemistry, University of Madras, Guindy Campus

Chennai – 600 025, INDIA

*Corresponding Author: Tel No: +91 44 2220 2814; E-Mail: perumalrajakumar@gmail.com 

 

Content

1NMR and 13C NMR of the compound 1, 2, 3, 5, 8, 9, 11 and 12 ………………..S-1

Mass Spectrum of the dendrimers 1, 2, 3.................................................................S-2

Antioxidant activity of the dendrimers 1, 2, 3…………………………………… S-3

 

 

 

 

 

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S-1

 

 

        1H NMR Spectrum (300MHz, CDCl3) of compound 5

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13C NMR spectrum (75MHz, CDCl3) of compound 5 

 

 

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                              1H NMR Spectrum (300MHz, DMSO-d6) of dendritic chloride 8

 

 

 

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13C NMR spectrum (75MHz, DMSO-d6) of dendritic chloride 8 

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                                         1H NMR Spectrum (300MHz, CDCl3) of dendritic azide 9

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13C NMR spectrum (75MHz, CDCl3) of dendritic azide 9

 

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1H NMR Spectrum (300MHz, CDCl3) of phenolic dendron 11

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13C NMR spectrum (75MHz, CDCl3) of phenolic dendron 11

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                                         1H NMR Spectrum (300MHz, CDCl3) of the compound 12 

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13C NMR spectrum (75MHz, CDCl3) of alkyne dendron 12

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                                          1H NMR Spectrum (300MHz, CDCl3) of dendrimer1

 

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13C NMR spectrum (75MHz, CDCl3) of dendrimer 1

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1H NMR Spectrum (300MHz, CDCl3) of dendrimer 2

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13C NMR spectrum (75MHz, CDCl3) of dendrimer 2

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1H NMR Spectrum (300MHz, CDCl3) of dendrimer 3

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13C NMR spectrum (75MHz, CDCl3) of dendrimer 3 

S-2

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Mass spectrum of dendrimer 1

[a.u.] x10

4 765.266

1244.506

Intens.

2.0

1723.577 [M+H]+

1.5

1.0

523.134

0.5

681.203

1389.910

0.0

500 750 1000 1250 1500 1750 2000 2250 2500 2750 m/z

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Mass Spectrum of dendrimer 2

Mass spectrum of dendrimer 2

[M+H]+

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Mass Spectrum of dendrimer 3

S-3

[M+H]+

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DPPH scavenging assay Method

Fig. S1 DPPH scavenging activity determined from the spectrophotometric assay are various

concentration of rhodamine B decorated dendrimer 1, 2 and 3

Fig.S2 DPPH scavenging capacities (EC50) of rhodamine B decorated dendrimer 1, 2 and 3

comparable with the standard viz., butylated hydroxyl toluene (BHT).

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20

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60

80

100

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20 40 60 80 100

DPPH Scavenging Activity (%

)

Concentration (µg/mL)

1

2

3

BHT

0

10

20

30

40

50

60

70

1 2 3 BHT

EC50value (µg/mL)

Dendrimers  

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Hydroxyl radical Scavenging Assay method

Fig. S3 Hydroxyl radical scavenging activity determined from the spectrophotometric assay with

various concentration of rhodamine B decorated dendrimer 1, 2 and 3

Fig. S4 Hydroxyl radical scavenging capacities (EC50) of rhodamine B decorated dendrimer 1, 2

and 3 comparable with the standard viz., Gallic Acid.

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10

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30

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70

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20 40 60 80 100

HO

.Scavenging Activity (%

)

Concentration (µg/mL)

1

2

3

Gallic Acid

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30

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50

60

70

1 2 3 Gallic acid

EC50value (µg/mL)

Dendrimers