US2009121031A1PendingUtilityA1
Method of minimizing visible coloration of substrate
Est. expiryApr 7, 2023(expired)· nominal 20-yr term from priority
Inventors:Lachlan Everett HallAlexandra Artemis PapadakisDamon Donald RidleyScott Matthew StarlingSimone Charlotte VonwillerKia SilverbrookPaul Lapstun
G06Q 30/0601G06Q 30/02H04N 25/778G06K 7/10722G06Q 30/0259G06Q 30/0207H04N 25/59G06K 7/10554G06Q 30/0267H04N 25/671G06F 3/0321G06Q 30/0212G06Q 30/0217G06Q 10/087G06Q 30/0236G06K 7/10623G06F 3/014G06Q 20/20G06K 7/10772G06K 7/10693H04N 25/767G06Q 10/00H04N 25/77H04N 25/78H04N 23/20H04N 25/7795
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Claims
Abstract
A method of minimizing visible coloration of a substrate having an IR-absorbing dye disposed thereon. The method includes preselecting the dye such that it includes a moiety for reducing intermolecular interactions between adjacent dye molecules.
Claims
exact text as granted — not AI-modified1 . A method of minimizing visible coloration of a substrate having an IR-absorbing dye disposed thereon, said method comprising preselecting said dye such that it includes a moiety for reducing intermolecular interactions between adjacent dye molecules.
2 . The method of claim 1 , wherein said dye is disposed in the form of a coded data pattern.
3 . The method of claim 1 , wherein said coded data pattern is a position-coding pattern.
4 . The method of claim 1 , wherein said substrate comprises an interface surface and wherein the coded data is disposed over a substantial portion of said interface surface.
5 . The method claim 1 , wherein said substrate is a paper sheet, a label, a tag, a packaging material or a product item.
6 . The method of claim 1 , wherein said dye is an IR-absorbing metal-dithiolene dye of formula (II):
wherein:
M is selected from Ni, Pd or Pt (preferably Ni);
j is selected from 1, 2, 3 or 4;
k is selected from 1, 2, 3 or 4;
n is 0, 1, 2 or 3;
W is selected from: a substituent comprising an ammonium group; a substituent comprising an acid group, including salts thereof, or a substituent comprising a sulfonamide group;
up to three —(CH 2 )— groups in the carbocycle are optionally replaced by a group independently selected from —C(O)—, —NH—, —S—, —O—;
up to three —CH— groups in the carbocycle may be optionally replaced by —N—; and
up to four H atoms in the carbocycle may be optionally replaced by a group independently selected from C 1-6 alkyl, C 1-6 alkoxy, C 5-12 aryl, C 5-12 arylalkyl, halogen, hydroxyl or amino.
7 . The method of claim 6 , wherein M is Ni.
8 . The method of claim 6 , wherein j is 1 and k is 2.
9 . The method of claim 6 , wherein n is 1.
10 . The method of claim 9 , wherein W is a substituent comprising a group of formula —CO 2 Z, —SO 3 Z, —OSO 3 Z, —PO 3 Z or —OPO 3 Z, wherein Z is H or a water-soluble cation.
11 . The method of claim 9 , wherein W is of formula —(CH 2 ) t —SO 3 Z, wherein t is 0 or an integer from 1 to 6, and Z is H or a water-soluble cation.
12 . The method of claim 9 , wherein W is of formula —CH 2 SO 3 H, —CH 2 SO 3 Na or —CH 2 SO 3 K.Cited by (0)
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