Material Science

The material science group main focus is the synthesis of polyethylene terephthalate (PET) and structural analoga for the study of the degradation mechanism including atomic force microscopy.

1. Synthesis of paranitrophenylesters in presence of triethylamine
2. Synthesis of polyethylene terephthalate in presence of sulfuric acid
3. Atomic force microscopy

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Synthesis of paranitrophnylesters with acyl chlorides in presence of triethylamine

Theory

The synthesis of the esters was achieved by combining acyl chlorides with paranitrophenole in presence of triethylamine. Acetone was used as solvent. The reaction takes 2 h at 0°C and inert conditions. Triethylamine is used as base to deprotonate paranitrophenol and to catalyze the attack of phenolate at the acyl chloride. It is dissipated by developing hydrogen chloride.

Preparation

Diparanitrophenyl succinate

In a 250 mL triple-neck round-bottom flask with reflux 6.79 g (48.82 mmol/ 2.01 eq.) paranitrophenole and 5.16 g (51.01 mmol/ 2.10 eq.) triethylamine are dissolved in 100 mL acetone under inert conditions and kept at 0 °C using a water/ice mixture. A solution of 1.70 g (10.07 mmol/ 1.00 eq.) succinyl chloride in 50 mL acetone is added dropwise with stirring 2 h at 0 °C. The resulting ester is precipitated in 400 mL distilled water, recrystallized from ethyl acetate three times and dried at 60 °C in a cabinet dryer over night. The yield is 2.3381 g (26.73 % of the theory).

Paranitrophenyl dihydrocinnamate

In a 100 mL triple-neck round-bottom flask with reflux 1.41 g (10.17 mmol/ 1.01 eq.) paranitrophenole and 1.07 g (10.57 mmol/ 1.05 eq.) triethylamine are dissolved in 50 mL acetone under inert conditions and kept at 0 °C using a water/ice mixture. A solution of 3.76 g (24.29 mmol/ 1.00 eq.) dihydrocinnamoyl chloride in 20 mL acetone is added dropwise with stirring 2 h at 0 °C. The resulting ester is precipitated in 200 mL distilled water, filtrated washed with ice cold acetone, stirred in distilled water for 2 h and dried at 60 °C in a cabinet dryer over night. The yield is 1.0623 g (34.69 % of the theory).

Analysis (¹H NMR-spectroscopy)

Diparanitrophenyl succinate

(300 MHz, CDCl₃): δ = 2.99 (2 H), 7.19-7.25 (2 H), 8.18-8.24 (2 H)

Paranitrophenyl dihydrocinnamate

(300 MHz, CDCl₃): δ = 2.94-2.97 (2 H), 3.07-3.10 (2 H), 7.18-7.21 (2 H), 7.26-7.35 (5 H), 8.24-8.28 (2 H)

Sources

• Thermoresponsive arginine-based hydrogels as biologic carriers 11.06.2009

Synthesis of polyethylene terephthalate in presence of sulfuric acid

Theory

To gain information about different methods of synthesis for Polyethylene terephthalate (PET) and the effect on physical and surface propieties, three experimets are done. The resulting oligo- and polymer is melted, cooled in liquid nitrogen and investigated with AFM. As the synthesis of polyethylene theephthalate is a reversible polykondensation of ethylene glycol and diemthyl terephthalate the developing methanol has to be removed from the reaction by destillation. Concentrated sulfuric acid is used as a catalyst.

Preparation

Conversion to polyethylene terephthalate 1

For the preparation of polyethylene terephthalate 2.73 g (14.05 mmol) of dimethylterephthalate were added to 43.68 mL (781.13 mmol) of ethylene glycol. After the addition of 2-3 drops of concentrated sulfuric acid the solution was heated under reflux at 65 °C for 20 min. After destilation of the Methanol, the resulting yellow solution was cooled for 48 hours at 5°C and filtered. White crystals were precipitated, they were washed with cold hexane and then with a little cold water. The dried crystals are melted at 80°C and poured on a flat metal plate. Which was immediately cooled to -210 °C. The resulting solid was investigated by atomic force microscopy.

Conversion to polyethylene terephthalate 2

For the preparation of polyethylene terephthalate 2.643 g (13.59 mmol) of dimethylterephthalate were added to 0.76 mL (13.59 mmol) of ethylene glycol in 50 mL DMSO. After the addition of 2-3 drops of concentrated sulfuric acid the solution was heated under reflux at 65 °C for 20 min. After destilation of the Methanol, the resulting yellow solution was cooled for 48 hours at 5°C and filtered. White crystals were precipitated, they were washed with cold hexane and then with a little cold water. The dried crystals are melted at 120 °C and poured on a flat metal plate. Which was immediately cooled to -210 °C. The resulting solid was investigated by atomic force microscopy.

Conversion to polyethylene terephthalate 3

For the preparation of polyethylene terephthalate 2.71 g (13.95 mmol) of dimethylterephthalate were added to 0.39 mL (0.69 mmol) of ethylene glycol in 50 mL DMSO. After the addition of 2-3 drops of concentrated sulfuric acid the solution was heated under reflux at 65 °C for 20 min. 0.39 mL (0.69 mmol) of ethylene glycol were added dropwise over 30 min. After destilation of the Methanol, the resulting yellow solution was cooled for 48 hours at 5 °C and filtered. White crystals were precipitated, they were washed with cold hexane and then with a little cold water. The dried crystals were melted at 170 °C. While reaching the temperature of 170 °C the crystals suplimated imediatly leading to a total loss of product.

Surface analysis of polyethylene terephthalate with atomic force microscopy (AFM)

Theory

Atomic force microscopy is used to make very precise surface analysis up to nanometer scale. The goal was to indentify differences between different modifications of polyethylene terephthalate and to proof enzymatic degradation by changed surface properties.

Testing

Experiment 1

Pieces of a PET water bottle are melted between two metal plates using a heat gun to create flat samples. They are incubated for 24 h after applying a solution of FsC and Est13. The Samples are washed with distilled water and dried in a cabinet dryer at 60 °C for 1 h. The samples are investigated using AFM. FsC induced surface modification of PET could be observed. There was no surface modification for Est13.

Experiment 2

Pieces of PET foil are added to solutions of FsC and Est13. In case of Est13 various concentrations are tested (50 mmol/L; 20 mmol/L; 2 mmol/L). After 7 days the samples are washed with distilled water and dried in a cabinet dryer at 60 °C over night. The samples are investigated using AFM. FsC induced surface modification of PET could be observed. There was no surface modification for no concentration of Est13. -->

Synthesis of paranitrophnylesters with acyl chlorides in presence of triethylamine

Introducion

The goal of the synthesis is to create paranitrophenylesters with similar polarity and sterical effects as PET-bricks. These are meant to be split enzymatically to deduce an enzymkinetic detecting cutingproducts.

Theory

The synthesis of the esters was achieved by combining acyl chlorides with paranitrophenole in presence of triethylamine. Acetone was used as solvent. The reaction takes 2 h at 0 °C and inert conditions. Triethylamine is used as base to deprotonate paranitrophenol and to catalyze the attack of phenolate at the acyl chloride. It is dissipated by developing hydrogen chloride.

Preparation

Diparanitrophenyl succinate

In a 250 mL triple-neck round-bottom flask with reflux 6.79 g (48.82 mmol/ 2.01 eq.) paranitrophenole and 5.16 g (51.01 mmol/ 2.10 eq.) triethylamine are dissolved in 100 mL acetone under inert conditions and kept at 0 °C using a water/ice mixture. A solution of 1.70 g (10.07 mmol/ 1.00 eq.) succinyl chloride in 50 mL acetone is added dropwise with stirring 2 h at 0 °C. The resulting ester is precipitated in 400 mL distilled water, recrystallized from ethyl acetate three times and dried at 60 °C in a cabinet dryer over night. The yield is 2.3381 g (26.73 % of the theory).

Paranitrophenyl dihydrocinnamate

In a 100 mL triple-neck round-bottom flask with reflux 1.41 g (10.17 mmol/ 1.01 eq.) paranitrophenole and 1.07 g (10.57 mmol/ 1.05 eq.) triethylamine are dissolved in 50 mL acetone under inert conditions and kept at 0 °C using a water/ice mixture. A solution of 3.76 g (24.29 mmol/ 1.00 eq.) dihydrocinnamoyl chloride in 20 mL acetone is added dropwise with stirring 2 h at 0 °C. The resulting ester is precipitated in 200 mL distilled water, filtrated washed with ice cold acetone, stirred in distilled water for 2 h and dried at 60 °C in a cabinet dryer over night. The yield is 1.0623 g (34.69 % of the theory).

Analysis (¹NMR-spectroscopy)

Diparanitrophenyl succinate

(300 MHz, CDCl₃): δ = 2.99 (2 H), 7.19-7.25 (2 H), 8.18-8.24 (2 H)

Paranitrophenyl dihydrocinnamate

(300 MHz, CDCl₃): δ = 2.94-2.97 (2 H), 3.07-3.10 (2 H), 7.18-7.21 (2 H), 7.26-7.35 (5 H), 8.24-8.28 (2 H)

Sources

Thermoresponsive arginine-based hydrogels as biologic carriers 11.06.2009

Synthesis of polyethylene terephthalate in presence of sulfuric acid

Theory

To gain information about different methods of synthesis for Polyethylene terephthalate (PET) and the effect on physical and surface propieties, three experimets are done. The resulting oligo- and polymer is melted, cooled in liquid nitrogen and investigated with AFM. As the synthesis of polyethylene theephthalate is a reversible polycondensation of ethylene glycol and diemthyl terephthalate the developing methanol has to be removed from the reaction by destillation. Concentrated sulfuric acid is used as a catalyst.

Preparation

Conversion to polyethylene terephthalate 1

For the preparation of polyethylene terephthalate 2.73 g (14.05 mmol) of dimethylterephthalate were added to 43.68 mL (781.13 mmol) of ethylene glycol. After the addition of 2-3 drops of concentrated sulfuric acid the solution was heated under reflux at 65 °C for 20 min. After destilation of the Methanol, the resulting yellow solution was cooled for 48 hours at 5°C and filtered. White crystals were precipitated, they were washed with cold hexane and then with a little cold water. The dried crystals are melted at 80°C and poured on a flat metal plate. Which was immediately cooled to -210 °C. The resulting solid was investigated by atomic force microscopy.

Conversion to polyethylene terephthalate 2

For the preparation of polyethylene terephthalate 2.643 g (13.59 mmol) of dimethylterephthalate were added to 0.76 mL (13.59 mmol) of ethylene glycol in 50 mL DMSO. After the addition of 2-3 drops of concentrated sulfuric acid the solution was heated under reflux at 65 °C for 20 min. After destilation of the Methanol, the resulting yellow solution was cooled for 48 hours at 5°C and filtered. White crystals were precipitated, they were washed with cold hexane and then with a little cold water. The dried crystals are melted at 120 °C and poured on a flat metal plate. Which was immediately cooled to -210 °C. The resulting solid was investigated by atomic force microscopy.

Conversion to polyethylene terephthalate 3

For the preparation of polyethylene terephthalate 2.71 g (13.95 mmol) of dimethylterephthalate were added to 0.39 mL (0.69 mmol) of ethylene glycol in 50 mL DMSO. After the addition of 2-3 drops of concentrated sulfuric acid the solution was heated under reflux at 65 °C for 20 min. 0.39 mL (0.69 mmol) of ethylene glycol were added dropwise over 30 min. After destilation of the Methanol, the resulting yellow solution was cooled for 48 hours at 5 °C and filtered. White crystals were precipitated, they were washed with cold hexane and then with a little cold water. The dried crystals were melted at 170 °C. While reaching the temperature of 170 °C the crystals suplimated imediatly leading to a total loss of product.

Atomic Force Microscopy (AFM)

Theory

AFM of FsC

exp1: File:AFM_FSC.jpg File:Optisch_FSC.png File:AFM_Referenz.jpg File:Optisch_Referenz.png exp2: Est13 2 File:3D_EST2_1.png File:AFM_EST2_1.jpg File:AFM_EST2_1_Amplitude_auto.jpg File:AFM_EST2_1_Phase.jpg 20 File:3D_EST20_2.png File:AFM_EST20_2_Amplitude.jpg File:AFM_EST20_2_Amplitude_auto.jpg File:AFM_EST20_2_Phase.jpg 50 File:3D_EST50.png File:AFM_EST50.jpg File:AFM_EST50_Amplitude_auto.jpg File:AFM_EST50_Phase.jpg FsC File:3D_FSC.png File:AFM_FSC_1.jpg File:AFM_FSC_1_Amplitude_auto.jpg File:AFM_FSC_1_Phase.jpg Reference File:3D_Referenz_2.png File:AFM_Referenz_1.jpg File:AFM_Referenz_1_Amplitude_auto.jpg File:AFM_Referenz_1_Phase.jpg

AFM of Est13