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Investigations on some selected conducting polymers and polymer ...

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Chapter-L<br />

<strong>polymer</strong>istai<strong>on</strong>, i<strong>some</strong>rizati<strong>on</strong>, Durham method, dehydrochlorinati<strong>on</strong> <strong>and</strong><br />

dehydrati<strong>on</strong> are used [9].<br />

A variety of techniques can be employed to get c<strong>on</strong>ducting<br />

<strong><strong>polymer</strong>s</strong> in thin film form. Soluti<strong>on</strong> casting, spin coating, plasma<br />

<strong>polymer</strong>izati<strong>on</strong> <strong>and</strong> electro chemical <strong>polymer</strong>izati<strong>on</strong> are <strong>some</strong> of the<br />

comm<strong>on</strong>ly used <strong>polymer</strong> thin film depositi<strong>on</strong> techniques [9,34-37].<br />

Soluti<strong>on</strong> cast films are prepared by dissolving definite amounts of the<br />

<strong>polymer</strong> in a <strong>selected</strong> suitable solvent. The mixture is stirred for several<br />

hours. The resulting soluti<strong>on</strong> is poured <strong>on</strong>to ultras<strong>on</strong>ically cleaned glass<br />

plates <strong>and</strong> spread uniformly using doctor's blade technique. The film is<br />

left to dry in a hot air/vacuum oven at about 70° C for <strong>on</strong>e or two days.<br />

Comm<strong>on</strong>ly used solvents are meta-cresol (m-cresol), N-Methyl<br />

Pyrrolidin<strong>on</strong>e (NMP), Para-cresol (p-cresol), Cyclohexanol <strong>and</strong> Xylene<br />

[9,36-37]. Metacresol is preferred over the rest because of its better<br />

solvati<strong>on</strong> properties. Also the <strong>polymer</strong>-solvent interacti<strong>on</strong>s are greater<br />

for the m-cresol soluti<strong>on</strong> compared to others[9,38].Still the solubility of<br />

c<strong>on</strong>ducting <strong><strong>polymer</strong>s</strong> in organic solvents remains a lot to be improved,<br />

the main reas<strong>on</strong> being the rigid <strong>polymer</strong> back b<strong>on</strong>e. The n c<strong>on</strong>jugati<strong>on</strong><br />

imparts stiffness to the <strong>polymer</strong> back b<strong>on</strong>e which makes the <strong>polymer</strong><br />

intractable. The Il electr<strong>on</strong> delocalizati<strong>on</strong> leads to large electr<strong>on</strong>ic<br />

polarizability, giving rise to Il- Il interchain attracti<strong>on</strong>. This favours<br />

<strong>polymer</strong> aggregati<strong>on</strong> rather than solvati<strong>on</strong>. Also the rigidity of the<br />

<strong>polymer</strong> back b<strong>on</strong>e thus formed creates an unfavourable entropy for<br />

soluti<strong>on</strong>. The <strong>polymer</strong> chains complexed with i<strong>on</strong>ic dopants also<br />

c<strong>on</strong>tain hydrophobic organic segments. It is very difficult to find

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