Poly(pyridinium salt)s with organic counterions derived from 3,3

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Poly(pyridinium salt)s with organic counterions derived from 3,3′-dimethylnaphthidine:

Thermal, liquid crystalline, and optical properties

Robin Jose, a* Dat Truong, a,1 Haesook Han, b and Pradip K. Bhowmik b a

Department of Natural Sciences, University of Houston-Downtown, One Main Street, Houston,

TX 77002-1001, USA., b

Department of Chemistry and Biochemistry, University of Nevada Las

Vegas, 4505 Maryland Parkway, Box 454003, Las Vegas, NV 89154-4003, USA.

* Correspondence to: Robin Jose (E-mail: Joser@uhd.edu

); Ph:+1 713-221-8115; Fax: +1713-

223-7476.

Fig. S1 FTIR spectrum of monomer 2 (film)

1

1 Department of Biochemistry and Biophysics

Texas A&M University

College of Agriculture and Life Sciences

2128 TAMU, College Station, TX 77843-2128

1

Fig. S2

1

H NMR spectrum of monomer 2 obtained in DMSOd

6

2

Fig. S3 13 C NMR spectrum of monomer 2 obtained in DMSOd

6

3

Fig S4 IR spectrum of polymer I (neat film cast from methanol)

4

Fig. S5 IR spectrum of polymer II (neat film cast from methanol)

5

Fig. S6 IR spectrum of polymer III (neat film cast from methanol)

6

Fig. S7 IR spectrum of polymer IV (neat film cast from methanol)

7

Fig. S8

1

H NMR spectrum of Polymer I obtained in DMSOd

6

8

Fig. S9 1 H NMR spectrum of Polymer II obtained in DMSOd

6

9

Fig. S10

1

H NMR spectrum of Polymer III obtained in DMSOd

6

10

Fig. S11

1

H NMR spectrum of Polymer IV obtained in DMSOd

6

11

Table S1. Molecular weights of poly(pyridinium salt)s containing 3,3′-dimethylnaphthidine moieties and organic counterions.

Polymer M n a

M w b

PDI c dn/dc (mL/g) R h

(nm) d

R g

(nm) e

I

II

56 74 1.32 0.0727

76

69

83

91

1.09

1.31

0.0940

0.0638 III

IV 56 72 1.30 a

Number-average molecular weight in kg/mol b

Weight-average molecular weight in kg/mol c Polydispersity index (M w

/M n

) d

Hydrodynamic radius e

Radius of gyration.

0.0746

10.2

10.8

11.0

10.2

13.4

14.1

14.3

13.3

12

Fig. S12 DSC thermograms of polymers I – IV in the second cooling cycles at the rate of 10

°C/min, under nitrogen

13

Fig. S13 UV-Vis spectra of polymers IIV obtained in acetonitrile

Fig. S14 UV-Vis spectra of polymers IIV obtained in methanol

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Table S2. Fluorescence properties of poly(pyridinium salt)s with various organic counterions.

I II III IV Polymer

PL λ em

(ACN)

572 543 572 543

(nm)

PL λ em

(MeOH) (nm)

PL λ em

(film a

)

(nm)

PL λ em

(film b

)

(nm)

556

511

511 a

Thin film cast from acetonitrile. b Thin film cast from methanol.

556

511

500

556

511

511

556

511

511

15

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