francesca d’anna,* h. q. nimal gunaratne, giuseppe lazzara, … · 2013. 7. 5. · 1 electronic...
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Electronic Supplementary Information
Solution and Thermal behaviour of Novel Dicationic Imidazolium Ionic Liquids
Francesca D’Anna,* H. Q. Nimal Gunaratne, Giuseppe Lazzara, Renato Noto,* Carla Rizzo
and Kenneth R. Seddon
Figure 1: 1H NMR spectra in dmso-d6 solution (0.038 M) in the range 300-390 K. Pages 2-6
Figure 2: 2D NOESY spectra of diimidazolium salts having aromatic dianions. Pages 7
Figure 3: DSC traces of dicationic functionalised salts. Pages 8
Figure 4: traces of TGA measurements. Pages 9
Figure 5: Plot of NMR linear correlation parameters as a function of Hm values corresponding to dicationic
functionalised salts 2a-i. Page 10
Electronic Supplementary Material (ESI) for Organic & Biomolecular ChemistryThis journal is © The Royal Society of Chemistry 2013
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Figure 1a: [2C8bti][Br]2 (2a)
Figure 1b: [2C8bti][BF4]2 (2b)
Electronic Supplementary Material (ESI) for Organic & Biomolecular ChemistryThis journal is © The Royal Society of Chemistry 2013
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Figure 1c: [2C8bti][NTf2]2 (2c)
Figure 1d: [2C8bti][2,6-nds] (2e)
Electronic Supplementary Material (ESI) for Organic & Biomolecular ChemistryThis journal is © The Royal Society of Chemistry 2013
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Figure 1e: [2C8bti][1,4-bdc] (2f)
Figure 1f: [2C8bti][2,6-ndc] (2g)
Electronic Supplementary Material (ESI) for Organic & Biomolecular ChemistryThis journal is © The Royal Society of Chemistry 2013
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Figure 1g: [2C8bti][ad] (2h)
Figure 1h: Expanded regions for [2C8bti][ad] (2h)
Electronic Supplementary Material (ESI) for Organic & Biomolecular ChemistryThis journal is © The Royal Society of Chemistry 2013
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Figure 1i: [2C8bti][sub] (2i)
Figure 1l: Expanded regions for [2C8bti][sub] (2i)
Figure 1: 1H NMR spectra in dmso-d6 solution (0.038 M) in the range 300-390 K relevant to dicationic functionalised
salts 2a-i.
Electronic Supplementary Material (ESI) for Organic & Biomolecular ChemistryThis journal is © The Royal Society of Chemistry 2013
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Figure 2. 2D NOESY spectra of dicationic functionalised salts: (a) [2C8bti][2,6-nds] (2e); (b)[2C8bti][1,4-bdc] (2f).
(a)
(b)
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Figure 3. DSC traces of dicationic functionalised salts: (a) [2C8bti][BF4]2 (2b); (b) [2C8bti][NTf2]2 (2c); (c) [2C8bti][1,5-nds] (2d); (d) [2C8bti][[2,6-nds] (2e); (e) [2C8bti][1,4-bdc] (2f); (f) [2C8bti][ad] (2h); (g) [2C8bti][sub] (2i).
(a) (b)
(c) (d)
(e) (f)
(g)
Electronic Supplementary Material (ESI) for Organic & Biomolecular ChemistryThis journal is © The Royal Society of Chemistry 2013
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Figure 4. Traces of TGA measurements relevant to dicationic functionalised salts: (a) [2C8bti][BF4]2 (2b); (b)
[2C8bti][NTf2]2 (2c); (c) [2C8bti][1,5-nds] (2d); (d) [2C8bti][[2,6-nds] (2e); (e) [2C8bti][1,4-bdc] (2f); (f) [2C8bti][2,6-
ndc] (2g); (g) [2C8bti][ad] (2h); (h) [2C8bti][sub] (2i).
(a)
(b)
(c) (d)
(e)
(f)
(g)
(h)
Electronic Supplementary Material (ESI) for Organic & Biomolecular ChemistryThis journal is © The Royal Society of Chemistry 2013
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0
1
2
3
4
5
6
0 1 0 2 0 3 0 4 0 5 0
[m o n o ] m 1 x 1 E 4
[d i] m 1 x 1 E 4
10
4 *
m1
(p
pm
/K)
Hm
(k J / m o l)
Figure 5. Plot of NMR linear correlation parameters as a function of Hm values corresponding to dicationic
functionalised salts.
Electronic Supplementary Material (ESI) for Organic & Biomolecular ChemistryThis journal is © The Royal Society of Chemistry 2013