http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2531088-A1

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filingDate 2004-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_688c0aaa4867375e302556c30847f242
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_127bba895c06090d4fe43eceb8154e07
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ebcb4587b5db1268518a15c08f57804b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_01226653c355e1c3aecb7974c3ed5cf3
publicationDate 2005-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2531088-A1
titleOfInvention Photochromic compounds
abstract Various non-limiting embodiments disclosed herein relate generally to photochromic compounds, which may be thermally reversible or non-thermally reversible, and articles made therefrom. Other non-limiting embodiments relate to photochromic-dichroic compounds, which may be thermally reversible or non-thermally reversible, and articles made therefrom. For example, one non-limiting embodiment provides a thermally reversible, photochromic compound adapted to have at least a first state and a second state, wherein the thermally reversible, photochromic compound has an average absorption ratio greater than 2.3 in at least one state as determined according to CELL METHOD. Another non-limiting embodiment provides a photochromic compound comprising: (a) at least one photochromic group chosen from a pyran, an oxazine, and a fulgide; and (b) at least one lengthening agent L attached to the at least one photochromic group and represented by the formula -[S1]c -[Q1-[S2]d ]d~-[Q2 -[S3]e~]e~ -[Q3 - [S4]f ]f -S5-P, which is described herein.
priorityDate 2003-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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