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Page 28

Note:

Biotechnology Congress 2018 & Emerging Materials 2018

Biomedical Research

|

ISSN: 0976-1683

|

Volume 29

S e p t e m b e r 0 6 - 0 7 , 2 0 1 8 | B a n g k o k , T h a i l a n d

allied

academies

Joint Event on

EMERGING MATERIALS AND NANOTECHNOLOGY

BIOTECHNOLOGY

&

Annual Congress on

Global Congress on

Vega Lloveras et al., Biomed Res 2018, Volume 29 | DOI: 10.4066/biomedicalresearch-C4-010

TUNING RADICAL INTERACTIONS IN PPH

RADICAL DENDRIMERS

Vega Lloveras, Flonja Liko, Luiz F Pinto

and

José Vidal Gancedo

Institut de Ciència de Materials de Barcelona ICMAB–CSIC, Spain

T

he spin-spin interactions between unpaired electrons in organic diradicals

and polyradicals are of crucial importance in many areas, such as organic

magnetism, molecular charge transfer, and multiple spin labeling in structural

biology. The flexibility of the scaffold and the length of the linker between

the unpaired electrons is expected to determine the extension of the spin

exchange coupling. Thus, the properties of the scaffold must be carefully

considered, when studying the spin-spin interactions in polyradicals. In

this context, we have turned our attention to dendrimers, whose end-

groups have been coupled to spin probes, allowing their study by electron

paramagnetic resonance spectroscopy (EPR). To discover in what magnitude

the spin exchange coupling could be tuned by changing the properties of

the linker between the radicals and the dendrimer, two generations (G

0

, G

1

)

of polyphosphorhydrazone (PPH) dendrimers were synthesized and fully

functionalized with pendant TEMPO radicals via acrylamido (G

n

-acrylamido-

TEMPO) or imino (G

n

-imino-TEMPO) group linkers. The EPR and cyclic

voltammetry (CV) studies showed that there existed much higher interactions

amongpendant group radicals, whenbounded to the dendrimer by iminogroup

linkers. This was true in either polar or less polar solvents. To conclude, we

were able to drastically change the way that the pendant radicals interacted,

by the solely substitution of the dendritic radical linker.

Vega Lloveras completed her PhD at the Autònoma

University of Barcelona, Spain, in 2006. She has a

permanent position at the Material Science Institute

of Barcelona (ICMAB-CSIC, Spain) in charge of some

spectroscopic equipment like Electron Paramagnetic

Resonance (EPR). She has 40 publications that have

been cited over 1450 times, and her publication H-in-

dex is 18.

vega@icmab.es

BIOGRAPHY