Tris(hydroxyphenyl)ethane benzotriazole: A copolymerizable UV light stabilizer

Citation
D. Kuila et al., Tris(hydroxyphenyl)ethane benzotriazole: A copolymerizable UV light stabilizer, CHEM MATER, 11(1), 1999, pp. 109-116
Citations number
49
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science","Material Science & Engineering
Journal title
CHEMISTRY OF MATERIALS
ISSN journal
08974756 → ACNP
Volume
11
Issue
1
Year of publication
1999
Pages
109 - 116
Database
ISI
SICI code
0897-4756(199901)11:1<109:TBACUL>2.0.ZU;2-L
Abstract
A novel UV-light stabilizer (UVLS), 3'-(2H-benzotriazol-2"-yl)-1,1,1-tris(4 '-hydroxyphenyl)ethane or simply tris(hydroxyphenyl)ethane benzotriazole (T HPE-BZT), that can be copolymerized with engineering plastic monomers has b een synthesized in three steps, The compound has two solid forms, a hydrate and an anhydrous form. Surprisingly, the hydrated form is more soluble in organic solvents such as acetone. Infrared spectra reveal that the hydrated form loses water of hydration upon heating and then forms a coplanar ring structure with a strong intramolecular hydrogen bond (IMHB) between one ben zotriazole nitrogen and the adjacent phenolic OH. The NMR and UV-vis spectr a in less polar organic solvents are also in accordance with the IMHB struc ture of THPE-BZT, In polar organic solvents such as DMSO and DMF and in MeO H/water at pH > 10, the IMHB is disrupted, and the disrupted form exists in equilibrium with the planar or nondisrupted form. However, THPE-BZT copoly merized into low molecular weight polysulfones and polycarbonates retains t he planar IMHB structure, as indicated by the UV absorption peak at similar to 335 nm, These copolymers have greater UV stability than those without a ny THPE-BZT because of dissipation of photon energy by molecular vibrationa l relaxation in the planar form. Also, polysulfone copolymers containing TH PE-BZT in the range of 0.25-1.5 mol % have greater UV light stability than polysulfone containing additive-type UVLS such as 2-(2'-hydroxy-5'-t-octylp henyl)benzotriazole (Cyasorb 5411). For polycarbonates, preliminary results show that copolymers of THPE-BZT have UV-light stability comparable to or only slightly less than that of polycarbonates blended with Cyasorb 5411 or THPE-BZT as additives. But the copolymers should escape the problems of su rface "blooming" and leaching by extraction experienced by noncopolymerized UVLS additives. Thermogravimetric analysis indicates that THPE-BZT is more stable than the commercial benzotriazoles 2-(2'-hydroxy-5'-methylphenyl)be nzotriazole (Tinuvin P), Cyasorb 5411, and the industrial standard-2-[2'-hy droxy-3',5'-bis ( 1-methyl-1-phenylethyl)phenyl]benzotriazole (Tinuvin 900) - and therefore might offer superior performance, even as an additive.