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Dms s14

Manufactured by Gelest

The DMS-S14 is a laboratory equipment product offered by Gelest. It is a specialized device designed for scientific and research applications. The core function of the DMS-S14 is to perform measurements and analysis, though the specific details of its intended use are not provided in this unbiased and factual description.

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4 protocols using dms s14

1

Synthesis of Aromatic Linked Siloxane-Based Triblock Copolymer

Check if the same lab product or an alternative is used in the 5 most similar protocols

Example 3

Synthesis of Aromatic Linked Siloxane Based Triblock Copolymer Pre-Soft-Segment:

[Figure (not displayed)]

To a 100 ml separable flask fitted with a mechanical stirrer, 15 g of hydroxy terminated polydimethyl siloxane (DMS-S14 from Gelest Inc.) was added along with 5.36 g of di-chloro p-xylene (from Sigma) and 0.0089 g of Copper(II) acetylacetonate (Cu(Acac)2 from Sigma). The reaction mixture was refluxed at 110° C. for 5 hrs. At this point, 19.77 g of hydroxy terminated poly(propylene glycol) (from Sigma) was added dropwise and the reaction mixture was then refluxed for another 15 hr. The progress of reaction was followed by 1H-NMR and the final molecular weight, determined by gel permeation chromatography (GPC), was 3000 g/mol.

H-NMR analysis; Solvent used for 1H-NMR analysis is CDCl3.

Aromatic H=7.25-7.45 ppm, —CH2=4.5-4.6 ppm, —CH3 (of PPO)=1-1.4 ppm, —CH2 (of PPO)=3.2-3.8 ppm, —OH (of PPO)=3.8-4 ppm, —CH3(silanol)=0.5-0.8 ppm.

TABLE 3
Resulting polymer block ratios
Stoiciometric ratios for reaction product:
Polymer block
POSiOPO
mnp
Ratio1415.514

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2

Synthesis of Aromatic Linked Siloxane-Based Triblock Copolymer

Check if the same lab product or an alternative is used in the 5 most similar protocols

Example 3

Synthesis of Aromatic Linked Siloxane Based Triblock Copolymer Pre-Soft-Segment:

[Figure (not displayed)]

To a 100 ml separable flask fitted with a mechanical stirrer, 15 g of hydroxy terminated polydimethyl siloxane (DMS-S14 from Gelest Inc.) was added along with 5.36 g of di-chloro p-xylene (from Sigma) and 0.0089 g of Copper(II) acetylacetonate (Cu(Acac)2 from Sigma). The reaction mixture was refluxed at 110° C. for 5 hrs. At this point, 19.77 g of hydroxy terminated poly(propylene glycol) (from Sigma) was added dropwise and the reaction mixture was then refluxed for another 15 hr. The progress of reaction was followed by 1H-NMR and the final molecular weight, determined by gel permeation chromatography (GPC), was 3000 g/mol.

H-NMR analysis: Solvent used for 1H-NMR analysis is CDCl3.

Aromatic H=7.25-7.45 ppm, —CH2=4.5-4.6 ppm, —CH3 (of PPO)=1-1.4 ppm, —CH2 (of PPO)=3.2-3.8 ppm, —OH (of PPO)=3.8-4 ppm, —CH3(silanol)=0.5-0.8 ppm.

TABLE 3
Resulting polymer block ratios
Stoiciometric ratios for reaction product:
Polymer block
POSiOPO
mnp
Ratio1415.514

+ Open protocol
+ Expand
3

Synthesis of Aromatic-Linked Siloxane Triblock Copolymer

Check if the same lab product or an alternative is used in the 5 most similar protocols

Example 3

Synthesis of Aromatic Linked Siloxane Based Triblock Copolymer Pre-Soft-Segment:

[Figure (not displayed)]

To a 100 ml separable flask fitted with a mechanical stirrer, 15 g of hydroxy terminated polydimethyl siloxane (DMS-S14 from Gelest Inc.) was added along with 5.36 g of di-chloro p-xylene (from Sigma) and 0.0089 g of Copper(II) acetylacetonate (Cu(Acac)2 from Sigma). The reaction mixture was refluxed at 110° C. for 5 hrs. At this point, 19.77 g of hydroxy terminated poly(propylene glycol) (from Sigma) was added dropwise and the reaction mixture was then refluxed for another 15 hr. The progress of reaction was followed by 1H-NMR and the final molecular weight, determined by gel permeation chromatography (GPC), was 3000 g/mol.

H-NMR analysis: Solvent used for 1H-NMR analysis is CDCl3.

Aromatic H=7.25-7.45 ppm, —CH2=4.5-4.6 ppm, —CH3 (of PPO)=1-1.4 ppm, —CH2 (of PPO)=3.2-3.8 ppm, —OH (of PPO)=3.8-4 ppm, —CH3(silanol)=0.5-0.8 ppm.

TABLE 3
Resulting polymer block ratios
Stoiciometric ratios for reaction product:
Polymer block
POSiOPO
mnp
Ratio1415.514

+ Open protocol
+ Expand
4

Synthesis of Aromatic-Linked Siloxane Triblock Copolymer

Check if the same lab product or an alternative is used in the 5 most similar protocols

Example 3

Synthesis of Aromatic Linked Siloxane Based Triblock Copolymer Pre-Soft-Segment:

[Figure (not displayed)]

To a 100 ml separable flask fitted with a mechanical stirrer, 15 g of hydroxy terminated polydimethyl siloxane (DMS-S14 from Gelest Inc.) was added along with 5.36 g of di-chloro p-xylene (from Sigma) and 0.0089 g of Copper(II) acetylacetonate (Cu(Acac)2 from Sigma). The reaction mixture was refluxed at 110° C. for 5 hrs. At this point, 19.77 g of hydroxy terminated poly(propylene glycol) (from Sigma) was added dropwise and the reaction mixture was then refluxed for another 15 hr. The progress of reaction was followed by 1H-NMR and the final molecular weight, determined by gel permeation chromatography (GPC), was 3000 g/mol.

H-NMR analysis: Solvent used for 1H-NMR analysis is CDCl3.

Aromatic H=7.25-7.45 ppm, —CH2=4.5-4.6 ppm, —CH3 (of PPO)=1-1.4 ppm, —CH2 (of PPO)=3.2-3.8 ppm, —OH (of PPO)=3.8-4 ppm, —CH3(silanol)=0.5-0.8 ppm.

TABLE 3
Resulting polymer block ratios
Stoiciometric ratios for reaction product:
Polymer block
POSiOPO
mnp
Ratio1415.514

+ Open protocol
+ Expand

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