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1 tion that converts the polyCBL into a linear polyester.
2 e incorporation of C(16) monomers into cutin polyester.
3 t and the existence of an extended aliphatic polyester.
4 to give the corresponding highly alternating polyester.
5 uorescein during enzymatic hydrolysis of the polyester.
6 tween the structures and properties of these polyesters.
7 approach to generate well-defined functional polyesters.
8 lymerized into the corresponding unsaturated polyesters.
9 containing no protic groups into unsaturated polyesters.
10 lity to hydrolyse both natural and synthetic polyesters.
11 ion efficiency of semi-crystalline bio-based polyesters.
12 ed to convert dimethacrylates to unsaturated polyesters.
13 ng well-defined high molecular weight cyclic polyesters.
14 sis of increasingly complex and well-defined polyesters.
15 in several monomers of cell wall-associated polyesters.
16 for hydrolysis of small molecule esters and polyesters.
17 s a strategy to generate well-defined cyclic polyesters.
18 monomers derived from non-extractable lipid polyesters.
19 merous types of functionality onto aliphatic polyesters.
20 ethane generated the homologated nitroalkane-polyesters.
21 ted to produce hydrogen gas or biodegradable polyesters.
22 stalline ester-linked COFs related to common polyesters.
23 g the trehalose- and zwitterion- substituted polyesters.
24 ated to hydrolyze all structurally different polyesters.
25 o prepare clinically translatable degradable polyesters.1 A variety of functional groups have been in
26 d with disperse blue 3 and disperse blue 14, polyester 777 dyed with disperse red 1 and disperse red
28 es were overexpressed together the epidermal polyesters accumulated new C20 and C22 omega-hydroxyacid
29 finishes, acrylic melamine (clear coating), polyester acrylic melamine (white coating) automotive fi
30 pecifically, two isomeric arylene-ethynylene polyesters afforded significantly different product dist
31 ed (DB, 50%), and pseudodendritic (DB, 100%) polyesters allowing the establishment of architecture ca
32 achieved using a hybrid polydimethylsiloxane/polyester amperometric lab-on-a-chip (LOC) microsystem w
33 an oxidant mechanism, whereas the non-coated polyester analogue and the Pluronic F68 alone had no eff
35 e systematically investigated the effects of polyester and carboxylesterase structure on the hydrolys
36 this work highlights the importance of both polyester and carboxylesterase structure to enzymatic po
38 tic slings, particularly those made of woven polyester and other tightly woven material erode 15 time
39 ow reactors to rapidly generate libraries of polyester and polycarbonate homopolymers and block copol
40 imple but robust strategy to bond semiporous polyester and polycarbonate membranes between layers of
41 lcohol)(PVA) sizes for high-speed weaving of polyester and polyester/cotton yarns to substantially de
42 es were significantly greater in cotton than polyester and similar for BFRs and high molecular weight
43 conjugation of hydroxyl-containing agents to polyesters and formation of corresponding nanoparticles.
46 is of relevant general purpose and specialty polyesters and polyamides; some of them are currently de
47 ynthetic routes to convert these monomers to polyesters and polycarbonate, and the different end-of-u
50 of metal-free polymers, including aliphatic polyesters and polyethers, poly(alpha-peptoid)s, poly(me
51 me-mediated hydrolysis of aliphatic-aromatic polyesters and will therefore have important implication
63 pplication and success of hydroxy acid based polyesters as degradable sutures and controlled drug del
64 reaction are shown to be compatible with the polyester backbone, this method is a generally useful me
74 ide evidence for a critical role of GPAT5 in polyester biogenesis in seed coats and roots and for the
75 knockout mutant lines for genes involved in polyester biosynthesis (att1, fatB and gpat5) were exami
76 substrate specificities (1) strongly support polyester biosynthetic pathways in which acyl transfer t
78 d or distinguished unreacted monomers in the polyester bulk in contrast to acid-base titrations where
79 tive analysis of the hydrolysis of two model polyesters by eight different carboxylesterases revealed
80 the enzymatic hydrolysis of eight aliphatic polyesters by two fungal esterases (FsC and Rhizopus ory
81 roval of the fat substitute olestra (sucrose polyester) called for active postmarketing surveillance
82 er, monomer diversity in naturally occurring polyesters can be limited with respect to the design of
84 yl azide, namely CF3(CF2)7CH2CH2N3, to yield polyesters carrying long-chain alkylene segments in the
87 ed to a combination of temperature-dependent polyester chain flexibility and accessibility of the enz
89 Hydrolyzability increased with increasing polyester-chain flexibility as evidenced from difference
91 mutants in which the abundance of cutin, the polyester component of the cuticle, was strongly reduced
98 It was found that increasing the hydrophobic polyester content in the hydrogel reduced the swelling v
103 PVA and chemically modified starch sizes on polyester/cotton fabrics, and had relative weaving effic
104 izes for high-speed weaving of polyester and polyester/cotton yarns to substantially decrease environ
105 astic, and porous crosslinked urethane-doped polyester (CUPE) scaffold sheets that are bonded togethe
112 e research activities generated on aliphatic polyester dendritic architectures based on bis-MPA.
113 d lipase activity, and seven proteins showed polyester depolymerization activity against polylactic a
115 led the rapid synthesis of >130 lipocationic polyesters directly from functional monomers without pro
116 The other functionalities in the linear polyester do not participate in the nanoparticle formati
117 t cationic proto-peptides (depsipeptides and polyesters), either produced as mixtures from plausibly
122 d by dip-coating acrylic, cotton, nylon, and polyester fabrics from solutions of diluted rat blood.
123 elative weaving efficiency similar to PVA on polyester fabrics, although with 3- 6% lower add-on.
124 nsulation panel made by hemp fiber (85%) and polyester fiber (15%) in 1 m(2) of wall having a thermal
125 ere, in combination with the stainless steel/polyester fiber blended yarn, the polydimethylsiloxane-c
126 cs may explain the observed results in which polyester fibers and polyamide beads triggered the most
127 h) and chronic (8 d) effects of microplastic polyester fibers and polyethylene (PE) beads on freshwat
128 ber composites reported to date, the MOF-808/polyester fibers exhibit the highest rates of nerve agen
130 the effects of six different microplastics (polyester fibers, polyamide beads, and four fragment typ
131 ere aligned with an intermediary cut-through polyester film and then thermally laminated together at
133 by integrating cellulose paper and flexible polyester films as diagnostic biosensing materials with
134 olymer, and the laser-printing of toner onto polyester films has been shown to be effective for gener
135 tructure on the hydrolysis of nanometer-thin polyester films using a quartz-crystal microbalance with
136 een 20 and 1000 times more formaldehyde than polyester filters under similar RH and airflow condition
137 Formaldehyde emissions from fiberglass and polyester filters used in building heating, ventilation,
139 -brand clothing manufacturer (three majority polyester fleece, and one nylon shell with nonwoven poly
141 rs in the commercialization of the bio-based polyesters, for example polyhydroxyalkanoates synthesize
142 rably with commercial adhesives or bio-based polyester formulations but without the need for tackifie
143 caprolactone (hydrophobe) and an alternating polyester from succinic acid and an ether-substituted ep
144 s in which a CO2 laser is used to remove the polyester from the channel sections of the internal laye
147 he usage of ionic liquids for studying plant polyesters has advantages over conventional approaches,
154 ysis included increased water solubility and polyester hydrophilicity as well as shorter diol chain l
156 here is much less known on biodegradation of polyesters in natural and artificial anaerobic habitats.
159 understanding of biodegradation processes of polyesters in WWTPs where the extracellular enzymatic hy
160 er fleece, and one nylon shell with nonwoven polyester insulation) and one off-brand (100% polyester
166 d with the outer integument and a cutin-like polyester layer associated with the inner seed coat.
167 noparticles that have a gold core, an apolar polyester layer for drug loading, a polar PEO corona to
168 parel accounts for a large proportion of the polyester market, and synthetic jackets represent the br
169 y step during the breakdown of biodegradable polyester materials in natural and engineered systems.
170 functionalized well-defined 3-D nanoparticle polyester materials in targeted nanoscopic ranges with a
171 lcanivorax to clear marine environments from polyester materials of anthropogenic origin as well as o
172 rious functionalities or by mixing different polyester materials to achieve controlled amounts of spe
175 DL), a fluorogenic ester substrate, into the polyester matrix and on monitoring the enzymatic cohydro
176 for hydrolysis of the protective cutin lipid polyester matrix in plants and thus have been exploited
177 y epidermal cells and is composed of a cutin polyester matrix that is embedded and covered with cutic
179 ased with decreasing differences between the polyester melting temperatures and the experimental temp
183 nonrecyclable waste-including microplastics (polyester microfibers) and food-contaminated plastic-and
184 ted microfluidic system using a multilayered polyester microfluidic disc created through laser print,
185 n the portal trunk of C57BL6 adult mice with polyester microspheres, to ensure a bilateral and distal
186 aphy coupled with mass spectrometry of lipid polyester monomers confirmed a drastic decrease in aliph
188 ent the synthesis of discrete functionalized polyester nanoparticles in selected nanoscale size dimen
189 We report the synthesis and encapsulation of polyester nanosponge particles (NPs) co-loaded with tamo
190 nsely cross-linked and hydrolytically stable polyester networks with low soluble fractions can be obt
191 eting ligands are required, these functional polyester NPs provide an exciting alternative approach f
192 cells internalized both coated and uncoated polyester NPs to a similar extent, with uptake observed
194 structure and formation of this hydrophobic polyester of glycerol and hydroxy/epoxy fatty acids has
196 of apparently all plant cuticles is cutin, a polyester of hydroxy fatty acids; however, despite its u
200 vidual dye-modified copolymers, dye-modified polyesters offer advantages over physical entrapment of
204 enables the selective preparation of either polyesters or polycarbonates or copoly(ester-carbonates)
207 -poly(ethylene glycol) (PEG) based precision-polyester (P2s) platform, permitting 5-12 periodically s
208 ludge to hydrolyze the synthetic compostable polyester PBAT (poly(butylene adipate-co-butylene tereph
211 crylate) (PMMA), polyethylene terephthalate (polyester, PET), and PETG are explored as substrate opti
212 hate (polyP), and the amphiphilic, solvating polyester, poly-(R)-3-hydroxybutyrate, frequently associ
213 ach may be expanded to a wide range of other polyester, polyamide, and polyurethane platform material
214 al behavior, and degradability of long-chain polyester, polyamides, polyurethanes, polyureas, polyace
215 il biodegradable mulch films composed of the polyester polybutylene adipate-co-terephthalate (PBAT) a
217 Vaginal fluid specimens were collected via polyester/polyethylene terephthalate swabs every other m
219 lymers, such as polysaccharides, polyamides, polyesters, polyphosphates, extracellular DNA and protei
221 copy identified multiple polymers, including polyester, polypropylene, polyvinyl chloride and vinyl c
223 f oligomers indicates the presence of linear polyesters possibly formed via esterfication reactions o
226 e the synthesis of closely related sequenced polyesters prepared by entropy-driven ring-opening metat
228 well-defined and functionalizable aliphatic polyesters remains a key challenge in the advancement of
229 in wax and polycaprolactone, a biodegradable polyester reported for the first time floating in off-sh
231 ples to assess the degree of interference of polyester resin in the GC-MS and Carbon-IRMS signals of
232 molecular and isotopic biomarker analysis on polyester resin-impregnated sediment slabs from archaeol
234 a CO(2) laser to create the microchannel in polyester sheets containing a uniform layer of printed t
236 abundant and widespread monomer of the cutin polyester, show that the morphology of floral surfaces d
237 e overaccumulation of ferulate in lipophilic polyester significantly increased the tolerance of trans
238 on indium tin oxide-coated substrates (e.g., polyester) simply by solution-casting the ECL gel and br
241 ax in its natural environment, where natural polyesters such as polyhydroxyalkanoates (PHA) are produ
244 cal lengths of surgical suture (chromic gut, polyester suture, silk, and nylon suture) and control un
245 The number of colonies from both the Dacron polyester swabs and medium were significantly lower than
247 of cutin synthase-like (CUS) proteins act as polyester synthases with negligible hydrolytic activity.
248 as partners of fatty acyl oxidases in lipid polyester synthesis and indicate that their cooverexpres
249 ught molecular bases of alkane formation and polyester synthesis have allowed construction of nearly
252 esults reveal a conserved mechanism of cutin polyester synthesis in land plants, and suggest that ela
256 of the key requirements in semi-crystalline polyesters, synthetic or bio-based, is the control on cr
259 eads, and four fragment types: polyethylene, polyester terephthalate, polypropylene, and polystyrene)
261 microplastic fibers released from synthetic (polyester) textiles during simulated home washing under
262 normous potential for biodegrading aliphatic polyesters thanks to a unique and abundantly secreted al
264 lenge, we report the discovery of functional polyesters that are capable of delivering siRNA drugs se
265 lic anhydride comonomer results in amorphous polyesters that exhibit glass transition temperatures (T
266 cturally different ionic phthalic acid based polyesters (the number-average molecular weights (Mn) 17
267 al approach to study enzymatic hydrolysis of polyesters, the key step in their overall biodegradation
268 lthough aromatics are the minor component of polyesters, they play important role in the sealing func
269 n of changes in the masses and rigidities of polyester thin films during enzymatic hydrolysis using a
271 rovide biosynthetic access to alpha-branched polyesters to enrich the properties of bio-based sustain
272 as been shown to be effective for generating polyester-toner (PeT) microfluidic devices with channel
273 Here, we describe the use of inexpensive polyester-toner, rotation-driven microfluidic devices wi
275 lyethylene glycol (PEG-PBA-PEG) (1.0-4.0 mg) polyester triblock copolymer; food oil, using olive and
276 study was to apply an elastic, biodegradable polyester urethane urea (PEUU) cardiac patch onto subacu
279 he hydrolysis rates and extents of aliphatic polyesters varying in the length of their dicarboxylic a
280 ly(butylene adipate-co-terephthalate) (PBAT) polyesters varying in their terephthalate-to-adipate rat
281 pylene oxide, we synthesized semicrystalline polyesters via the copolymerization of a range of epoxid
285 h high performing zwitterionic and trehalose polyesters were also degraded, and the polymers and degr
286 ing the corresponding diacid chloride; these polyesters were quantitatively "clicked" with a fluoroal
287 ee types of swabs, flocked-nylon, rayon, and polyester, were evaluated by 3 extraction methods, the s
288 e highest HTP activity and also produced the polyester with the highest Mn, while the Cl-substituted
289 ontrolled coupling of epoxide functionalized polyesters with 2,2'-(ethylenedioxy)bis(ethylamine) to g
291 afford structurally and functionally diverse polyesters with controlled molecular weights and dispers
292 -based system rapidly converts gamma-BL into polyesters with high monomer conversions (up to 90 %), h
293 is a route to a new class of semicrystalline polyesters with improved properties, produced from readi
298 rovides access to a range of new unsaturated polyesters with versatile functionality, as well as the
300 e alkyne groups at high density in aliphatic polyesters without compromising their crystallinity via