Heat-mode recording medium

Claim 2

A heat-mode recording medium comprising: (a) a substrate and (b) a recording layer formed thereon comprising a thin film of an organic material having a regularly oriented crystallization direction which can be thermally and reversibly controlled, wherein said organic material is a fatty acid or fatty acid derivative having 10 or more carbon atoms.

Claim 3

The heat-mode recording medium as claimed in claim 1, wherein said organic material is crystallized by the steps of melting said organic material, supercooling said melted organic material and crystallizing said supercooled organic material in its entirely by further cooling said organic material locally.

Claim 4

The heat-mode recording medium as claimed in claim 1, wherein said crystallized organic material has an optical axis extending in a radial direction from a predetermined center thereof.

Claim 5

The heat-mode recording medium as claimed in claim 1, wherein said substrate is disc-shaped and said organic material consists of an aggregation of crystal domains.

Claim 6

The heat-mode recording medium as claimed in claim 4, wherein said crystal domains are directed in a radial direction from the center of said substrate.

Claim 7

The heat-mode recording medium as claimed in claim 4, wherein said crystal domains are directed in a tangential direction of concentric circles having its center at the center of said disc-shaped substrate.

Claim 8

The heat-mode recording medium as claimed in claim 1, wherein said organic material is a benzoic acid derivative having formula (I): ##STR2## wherein R 1 represents hydrogen, an alkyl group having 1 to 6 carbon atoms, which may have a substituent, an alkoxyl group having 1 to 6 carbon atoms, which may have a substituent, an aryl group which may have a substituent, an acyl group, an acyloxy group, a halogen, a nitro group, a hydroxyl group, a cyano group, a carboxyl group or an ester group thereof, a carbamoyl group which may have a substituent, a sulfo group or an ester group thereof, or an amino group which may have a substituent selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, a phenyl group and a substituted phenyl group.

Claim 9

The heat-mode recording medium as claimed in claim 7, wherein said substituent of said alkyl group, said alkoxyl group or said aryl group represented by R 1 is selected from the group consisting of an acyl group, an acyloxy group, a halogen, a nitro group, a hydroxyl group, a cyano group, a carboxyl group or an ester group thereof, a carbamoyl group which may have a substituent, a sulfo group or an ester group thereof, and an amino group which may have a substituent selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, a phenyl group and a substituted phenyl group.

Claim 10

The heat-mode recording medium as claimed in claim 1, wherein said organic material is a benzoic acid compound having formula (II): ##STR3## wherein R 1 represents hydrogen, an alkyl group having 1 to 6 carbon atoms, which may have a substituent, an alkoxyl group having 1 to 6 carbon atoms, which may have a substituent, an aryl group which may have a substituent, an acyl group, an acyloxy group, a halogen, a nitro group, a hydroxyl group, a cyano group, a carboxyl group or an ester group thereof, a carbamoyl group which may have a substituent, a sulfo group or an ester group thereof, or an amino group which may have a substituent selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, a phenyl group and a substituted phenyl group; and R 2 represents hydrogen, an alkyl group having 1 to 6 carbon atoms, which may have a substituent, an alkoxy group having 1 to 6 carbon atoms, which may have a substituent, or an aryl group which may have a substituent.

Claim 11

The heat-mode recording medium as claimed in claim 9, wherein said substituent of said alkyl group, said alkoxy group or said aryl group represented by R 1 is selected from the group consisting of an acyl group, an acyloxy group, a halogen, a nitro group, a hydroxyl group, a cyano group, a carboxyl group or an ester group thereof, a carbamoyl group which may have a substituent, a sulfo group or an ester group thereof, and an amino group which may have a substituent selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, a phenyl group and a substituted phenyl group.

Claim 12

The heat-mode recording medium as claimed in claim 1, wherein said organic material is a benzoic acid compound having formula (III): ##STR4## wherein R 1 represents hydrogen, an alkyl group having 1 to 6 carbon atoms, which may have a substituent, an alkoxyl group having 1 to 6 carbon atoms, which may have a substituent, an aryl group which may have a substituent, an acyl group, an acyloxy group, a halogen, a nitro group, a hydroxyl group, a cyano group, a carboxyl group or an ester group thereof, a carbamoyl group which may have a substituent, a sulfo group or an ester group thereof, or an amino group which may have a substituent selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, a phenyl group and a substituted phenyl group.

Claim 13

The heat-mode recording medium as claimed in claim 11, wherein said substituent of said alkyl group, said alkoxyl group or said aryl group represented by R 1 is selected from the group consisting of an acyl group, an acyloxy group, a halogen, a nitro group, a hydroxyl group, a cyano group, a carboxyl group or an ester group thereof, a carbamoyl group which may have a substituent, a sulfo group or an ester group thereof, and an amino group which may have a substituent selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, a phenyl group and a substituted phenyl group.

Claim 14

The heat-mode recording medium as claimed in claim 1, wherein said organic material is a benzoic acid compound having formula (IV): ##STR5## wherein R 1 represents hydrogen, an alkyl group having 1 to 6 carbon atoms, which may have a substituent, an alkoxyl group having 1 to 6 carbon atoms, which may have a substituent, an aryl group which may have a substituent, an acyl group, an acyloxy group, a halogen, a nitro group, a hydroxyl group, a cyano group, a carboxyl group or an ester group thereof, a carbamoyl group which may have a substituent, a sulfo group or an ester group thereof, or an amino group which may have a substituent selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, a phenyl group and a substituted phenyl group; and R 2 and R 3 each represent hydrogen, an alkyl group having 1 to 6 carbon atoms, which may have a substituent, an alkoxyl group having 1 to 6 carbon atoms, which may have a substituent, or an aryl group which may have a substituent.

Claim 15

The heat-mode recording medium as claimed in claim 13, wherein said substituent of said alkyl group, said alkoxyl group or said aryl group represented by R 1 is selected from the group consisting of an acyl group, an acyloxy group, a halogen, a nitro group, a hydroxyl group, a cyano group, a carboxyl group or an ester group thereof, a carbamoyl group which may have a substituent, a sulfo group or an ester group thereof, and an amino group which may have a substituent selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, a phenyl group and a substituted phenyl group.

Claim 16

The heat-mode recording medium as claimed in claim 1, wherein said organic material is a n-alkane derivative having a melting point of 50° C. or more.

Claim 17

The heat-mode recording medium as claimed in claim 1, wherein said fatty acid is a saturated or unsaturated mono- or di-carboxylic acid.

Claim 18

The heat-mode recording medium as claimed in claim 1, wherein said fatty acid derivative is an ester of a saturated or unsaturated mono- or di-carboxylic acid.

Claim 19

The heat-mode recording medium as claimed in claim 1, wherein said fatty acid derivative is an amide of a saturated or unsaturated mono- or di-carboxylic acid.

Claim 20

The heat-mode recording medium as claimed in claim 1, wherein said fatty acid derivative is an anilide of a saturated or unsaturated mono- or di-carboxylic acid.

Claim 21

The heat-mode recording medium as claimed in claim 1, wherein said fatty acid derivative is a hydrazide of a saturated or unsaturated mono- or di-carboxylic acid.

Claim 22

The heat-mode recording medium as claimed in claim 1, wherein said fatty acid derivative is an ureido derived from a saturated or unsaturated mono- or di-carboxylic acid.

Claim 23

The heat-mode recording medium as claimed in claim 1, wherein said fatty acid derivative is an anhydride of a saturated or unsaturated mono- or di-carboxylic acid.

Claim 24

The heat-mode recording medium as claimed in claim 1, wherein said fatty acid derivative is an ammonium salt of a saturated or unsaturated mono- or di-carboxylic acid.

Claim 25

The heat-mode recording medium as claimed in claim 1, wherein said fatty acid derivative is a metal salt of a saturated or unsaturated mono- or di-carboxylic acid.

Claim 26

The heat-mode recording medium as claimed in claim 1, wherein said recording layer is formed by the steps of fusing said organic material with application of heat thereto to form a fused portion in said recording layer, and subsequently cooling said fused portion in such a fashion that the crystallization direction of said organic material in said recording layer is oriented in a predetermined direction.

Claim 27

The heat-mode recording medium as claimed in claim 1, wherein said recording layer is formed by the steps of fusing said organic material in said recording layer in its entirety with application of heat thereto, and subsequently cooling a predetermined point of said recording layer in such a fashion that the crystallization direction of said organic material in said recording layer is oriented in a predetermined direction.

Claim 28

The heat-mode recording medium as claimed in claim 1, wherein said recording layer is formed by the steps of fusing said organic material in said recording layer in its entirety with application of heat thereto, supercooling said fused recording layer, and subsequently cooling a predetermined point of said recording layer in such a fashion that the crystallization direction of said organic material in said recording layer is oriented in a predetermined direction.