ThuliumV1, Pascal, Curation, bibRecord, 000561

Influence of the hydroxyl groups on the properties of hydrazone based molecular glasses

Identifieur interne : 000561 ( Pascal/Curation ); précédent : 000560; suivant : 000562

Influence of the hydroxyl groups on the properties of hydrazone based molecular glasses

Auteurs : Vytautas Getautis [Lituanie] ; Maryte Daskeviciene [Lituanie] ; Tadas Malinauskas [Lituanie] ; Vygintas Jankauskas [Lituanie] ; Jonas Sidaravicius [Lituanie]

Source :

Thin solid films [ 0040-6090 ] ; 2008.

RBID : Pascal:09-0041603

Descripteurs français

Pascal (Inist)
- Groupe hydroxyle, Hydrazone, Verre, Conductivité type p, Chromophore, Structure moléculaire, Couche mince, Calorimétrie différentielle balayage, Méthode temps vol, Plan expérience, Semiconducteur organique, Transport charge, Relation structure propriété, Sulfure de thulium, Verre organique, S Tm, TmS, 8105K, 8140L.
Wicri :
- topic : Verre.

English descriptors

KwdEn :
- Charge transport, Chromophore, Differential scanning calorimetry, Experimental design, Glass, Hydrazone, Hydroxyl group, Molecular structure, Organic glass, Organic semiconductors, P type conductivity, Property structure relationship, Thin film, Thulium sulfides, Time of flight method.

Abstract

The novel family of the hydrazone based hole transporting materials possessing different amount and position of hydroxyl groups in the linking fragment of photoconductive chromophores were synthesized and investigated as potential new materials for electrophotography. The molecular structure of these hole transporting materials (TM) ensures good compatibility with hydroxyl groups containing binding material (BM) polivinylbutyral (PVB) and allows stable films to be prepared. Obtained compounds were characterized by differential scanning calorimetry (DSC) and time of flight method. Unlike a significant influence on the morphological properties, the position of the hydroxyl groups towards each other does not influence the mobility values of investigated TMs.

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A02	`01`			`@0 THSFAP`
A03		`1`		`@0 Thin solid films`
A05				`@2 516`
A06				`@2 24`
A08	`01`	`1`	`ENG`	`@1 Influence of the hydroxyl groups on the properties of hydrazone based molecular glasses`
A09	`01`	`1`	`ENG`	`@1 The Tenth European Conference on Organised Films (ECOF-10)`
A11	`01`	`1`		`@1 GETAUTIS (Vytautas)`
A11	`02`	`1`		`@1 DASKEVICIENE (Maryte)`
A11	`03`	`1`		`@1 MALINAUSKAS (Tadas)`
A11	`04`	`1`		`@1 JANKAUSKAS (Vygintas)`
A11	`05`	`1`		`@1 SIDARAVICIUS (Jonas)`
A12	`01`	`1`		`@1 MUZIKANTE (Inta) @9 ed.`
A14	`01`			`@1 Department of Organic Chemistry, Kaunas University of Technology, Radvilenu pl. 19 @2 50270 Kaunas @3 LTU @Z 1 aut. @Z 2 aut. @Z 3 aut.`
A14	`02`			`@1 Department of Solid State Electronics, Vilnius University, Sauletekio 9 @2 10222 Vilnius @3 LTU @Z 4 aut.`
A14	`03`			`@1 Department of Polygraphic Machines, Vilnius Gediminas Technical University, J Basanaviciaus str. 28 @2 03224, Vilnius @3 LTU @Z 5 aut.`
A15	`01`			`@1 Institute of Solid State Physics, University of Latvia, Kengaraga Str. 8 @2 Riga, 1063 @3 LVA @Z 1 aut.`
A20				`@1 8979-8983`
A21				`@1 2008`
A23	`01`			`@0 ENG`
A43	`01`			`@1 INIST @2 13597 @5 354000184294320270`
A44				`@0 0000 @1 © 2009 INIST-CNRS. All rights reserved.`
A45				`@0 30 ref.`
A47	`01`	`1`		`@0 09-0041603`
A60				`@1 P @2 C`
A61				`@0 A`
A64	`01`	`1`		`@0 Thin solid films`
A66	`01`			`@0 CHE`
C01	`01`		`ENG`	@0 The novel family of the hydrazone based hole transporting materials possessing different amount and position of hydroxyl groups in the linking fragment of photoconductive chromophores were synthesized and investigated as potential new materials for electrophotography. The molecular structure of these hole transporting materials (TM) ensures good compatibility with hydroxyl groups containing binding material (BM) polivinylbutyral (PVB) and allows stable films to be prepared. Obtained compounds were characterized by differential scanning calorimetry (DSC) and time of flight method. Unlike a significant influence on the morphological properties, the position of the hydroxyl groups towards each other does not influence the mobility values of investigated TMs.
C02	`01`	`X`		`@0 001D03C`
C03	`01`	`X`	`FRE`	`@0 Groupe hydroxyle @5 01`
C03	`01`	`X`	`ENG`	`@0 Hydroxyl group @5 01`
C03	`01`	`X`	`SPA`	`@0 Grupo hidróxilo @5 01`
C03	`02`	`X`	`FRE`	`@0 Hydrazone @5 02`
C03	`02`	`X`	`ENG`	`@0 Hydrazone @5 02`
C03	`02`	`X`	`SPA`	`@0 Hidrazona @5 02`
C03	`03`	`X`	`FRE`	`@0 Verre @5 03`
C03	`03`	`X`	`ENG`	`@0 Glass @5 03`
C03	`03`	`X`	`SPA`	`@0 Vidrio @5 03`
C03	`04`	`X`	`FRE`	`@0 Conductivité type p @5 04`
C03	`04`	`X`	`ENG`	`@0 P type conductivity @5 04`
C03	`04`	`X`	`SPA`	`@0 Conductividad tipo p @5 04`
C03	`05`	`X`	`FRE`	`@0 Chromophore @5 05`
C03	`05`	`X`	`ENG`	`@0 Chromophore @5 05`
C03	`05`	`X`	`SPA`	`@0 Cromóforo @5 05`
C03	`06`	`X`	`FRE`	`@0 Structure moléculaire @5 06`
C03	`06`	`X`	`ENG`	`@0 Molecular structure @5 06`
C03	`06`	`X`	`SPA`	`@0 Estructura molecular @5 06`
C03	`07`	`X`	`FRE`	`@0 Couche mince @5 07`
C03	`07`	`X`	`ENG`	`@0 Thin film @5 07`
C03	`07`	`X`	`SPA`	`@0 Capa fina @5 07`
C03	`08`	`X`	`FRE`	`@0 Calorimétrie différentielle balayage @5 08`
C03	`08`	`X`	`ENG`	`@0 Differential scanning calorimetry @5 08`
C03	`08`	`X`	`SPA`	`@0 Análisis calorimétrico barrido exploración @5 08`
C03	`09`	`X`	`FRE`	`@0 Méthode temps vol @5 09`
C03	`09`	`X`	`ENG`	`@0 Time of flight method @5 09`
C03	`09`	`X`	`SPA`	`@0 Método tiempo vuelo @5 09`
C03	`10`	`X`	`FRE`	`@0 Plan expérience @5 10`
C03	`10`	`X`	`ENG`	`@0 Experimental design @5 10`
C03	`10`	`X`	`SPA`	`@0 Plan experiencia @5 10`
C03	`11`	`3`	`FRE`	`@0 Semiconducteur organique @5 11`
C03	`11`	`3`	`ENG`	`@0 Organic semiconductors @5 11`
C03	`12`	`3`	`FRE`	`@0 Transport charge @5 12`
C03	`12`	`3`	`ENG`	`@0 Charge transport @5 12`
C03	`13`	`X`	`FRE`	`@0 Relation structure propriété @5 13`
C03	`13`	`X`	`ENG`	`@0 Property structure relationship @5 13`
C03	`13`	`X`	`SPA`	`@0 Relación estructura propiedad @5 13`
C03	`14`	`3`	`FRE`	`@0 Sulfure de thulium @2 NK @5 15`
C03	`14`	`3`	`ENG`	`@0 Thulium sulfides @2 NK @5 15`
C03	`15`	`X`	`FRE`	`@0 Verre organique @5 16`
C03	`15`	`X`	`ENG`	`@0 Organic glass @5 16`
C03	`15`	`X`	`SPA`	`@0 Vidrio orgánico @5 16`
C03	`16`	`X`	`FRE`	`@0 S Tm @4 INC @5 46`
C03	`17`	`X`	`FRE`	`@0 TmS @4 INC @5 47`
C03	`18`	`X`	`FRE`	`@0 8105K @4 INC @5 71`
C03	`19`	`X`	`FRE`	`@0 8140L @4 INC @5 72`
N21				`@1 026`

A30	`01`	`1`	`ENG`	`@1 European Conference on Organised Films (ECOF-10) @2 10 @3 Riga LVA @4 2006-08-21`

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Le document en format XML

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<term>Hydrazone</term>
<term>Hydroxyl group</term>
<term>Molecular structure</term>
<term>Organic glass</term>
<term>Organic semiconductors</term>
<term>P type conductivity</term>
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<term>Structure moléculaire</term>
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<term>Méthode temps vol</term>
<term>Plan expérience</term>
<term>Semiconducteur organique</term>
<term>Transport charge</term>
<term>Relation structure propriété</term>
<term>Sulfure de thulium</term>
<term>Verre organique</term>
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<front><div type="abstract" xml:lang="en">The novel family of the hydrazone based hole transporting materials possessing different amount and position of hydroxyl groups in the linking fragment of photoconductive chromophores were synthesized and investigated as potential new materials for electrophotography. The molecular structure of these hole transporting materials (TM) ensures good compatibility with hydroxyl groups containing binding material (BM) polivinylbutyral (PVB) and allows stable films to be prepared. Obtained compounds were characterized by differential scanning calorimetry (DSC) and time of flight method. Unlike a significant influence on the morphological properties, the position of the hydroxyl groups towards each other does not influence the mobility values of investigated TMs.</div>
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<s9>ed.</s9>
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<fA14 i1="01"><s1>Department of Organic Chemistry, Kaunas University of Technology, Radvilenu pl. 19</s1>
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<fA14 i1="02"><s1>Department of Solid State Electronics, Vilnius University, Sauletekio 9</s1>
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<s3>LTU</s3>
<sZ>5 aut.</sZ>
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<fA15 i1="01"><s1>Institute of Solid State Physics, University of Latvia, Kengaraga Str. 8</s1>
<s2>Riga, 1063</s2>
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<fC01 i1="01" l="ENG"><s0>The novel family of the hydrazone based hole transporting materials possessing different amount and position of hydroxyl groups in the linking fragment of photoconductive chromophores were synthesized and investigated as potential new materials for electrophotography. The molecular structure of these hole transporting materials (TM) ensures good compatibility with hydroxyl groups containing binding material (BM) polivinylbutyral (PVB) and allows stable films to be prepared. Obtained compounds were characterized by differential scanning calorimetry (DSC) and time of flight method. Unlike a significant influence on the morphological properties, the position of the hydroxyl groups towards each other does not influence the mobility values of investigated TMs.</s0>
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<fC02 i1="01" i2="X"><s0>001D03C</s0>
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<s5>02</s5>
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<s5>03</s5>
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<s5>04</s5>
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<s5>04</s5>
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<fC03 i1="05" i2="X" l="FRE"><s0>Chromophore</s0>
<s5>05</s5>
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<fC03 i1="05" i2="X" l="ENG"><s0>Chromophore</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Cromóforo</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE"><s0>Structure moléculaire</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG"><s0>Molecular structure</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA"><s0>Estructura molecular</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE"><s0>Couche mince</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG"><s0>Thin film</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA"><s0>Capa fina</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE"><s0>Calorimétrie différentielle balayage</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG"><s0>Differential scanning calorimetry</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA"><s0>Análisis calorimétrico barrido exploración</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE"><s0>Méthode temps vol</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG"><s0>Time of flight method</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA"><s0>Método tiempo vuelo</s0>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE"><s0>Plan expérience</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG"><s0>Experimental design</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA"><s0>Plan experiencia</s0>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="3" l="FRE"><s0>Semiconducteur organique</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="3" l="ENG"><s0>Organic semiconductors</s0>
<s5>11</s5>
</fC03>
<fC03 i1="12" i2="3" l="FRE"><s0>Transport charge</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="3" l="ENG"><s0>Charge transport</s0>
<s5>12</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE"><s0>Relation structure propriété</s0>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG"><s0>Property structure relationship</s0>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA"><s0>Relación estructura propiedad</s0>
<s5>13</s5>
</fC03>
<fC03 i1="14" i2="3" l="FRE"><s0>Sulfure de thulium</s0>
<s2>NK</s2>
<s5>15</s5>
</fC03>
<fC03 i1="14" i2="3" l="ENG"><s0>Thulium sulfides</s0>
<s2>NK</s2>
<s5>15</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE"><s0>Verre organique</s0>
<s5>16</s5>
</fC03>
<fC03 i1="15" i2="X" l="ENG"><s0>Organic glass</s0>
<s5>16</s5>
</fC03>
<fC03 i1="15" i2="X" l="SPA"><s0>Vidrio orgánico</s0>
<s5>16</s5>
</fC03>
<fC03 i1="16" i2="X" l="FRE"><s0>S Tm</s0>
<s4>INC</s4>
<s5>46</s5>
</fC03>
<fC03 i1="17" i2="X" l="FRE"><s0>TmS</s0>
<s4>INC</s4>
<s5>47</s5>
</fC03>
<fC03 i1="18" i2="X" l="FRE"><s0>8105K</s0>
<s4>INC</s4>
<s5>71</s5>
</fC03>
<fC03 i1="19" i2="X" l="FRE"><s0>8140L</s0>
<s4>INC</s4>
<s5>72</s5>
</fC03>
<fN21><s1>026</s1>
</fN21>
</pA>
<pR><fA30 i1="01" i2="1" l="ENG"><s1>European Conference on Organised Films (ECOF-10)</s1>
<s2>10</s2>
<s3>Riga LVA</s3>
<s4>2006-08-21</s4>
</fA30>
</pR>
</standard>
</inist>
</record>

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Influence of the hydroxyl groups on the properties of hydrazone based molecular glasses

Influence of the hydroxyl groups on the properties of hydrazone based molecular glasses

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