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1.
The allomerization of chlorophyll b in methanol produced 132(S)-hydroxy-10-methoxychlorophyll b in a yield of ca. 8%. The formation of this allomer was totally unexpected, as 10-substituted chlorophylls have never been reported before. The structure of the new chlorophyll b derivative was determined on the basis of UV/Vis, FAB-MS, 1H NMR and 2D ROESY NMR spectra. This letter focuses on the NMR analysis. 相似文献
2.
The regio- and stereospecific glycosylation of 8,3′,5′-trideuterodaidzein 1 with α-acetobromoglucose to provide 8,3′,5′-trideuterodaidzein-7-O-β-glucopyranoside 2 is presented. 相似文献
3.
Kalevi Pihlaja Pentti Oksman Gza Stjer Gbor Bernth 《Journal of mass spectrometry : JMS》1990,25(2):115-118
A mass spectrometric identification and differentiation of pyrimidin-4(3H)- and -4(1H)-ones was carried out. N-Substitution at position 1 or 3 made the distinction of the two sets of compounds very easy because of their characteristic fragmentation pathways. Most interesting were the spectra of the N-unsubstituted derivatives, which illustrated a predominance of the two possible NH tautomers in relation to the 4-hydroxy structure. 相似文献
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5.
Mehdi Jonoobi Jalaluddin Harun Aji P. Mathew Mohd Zobir B. Hussein Kristiina Oksman 《Cellulose (London, England)》2010,17(2):299-307
The aim of this study was to develop cellulose nanofibers with hydrophobic surface characteristics using chemical modification.
Kenaf fibers were modified using acetic anhydride and cellulose nanofibers were isolated from the acetylated kenaf using mechanical
isolation methods. Fourier transform infrared spectroscopy (FTIR) indicated acetylation of the hydroxyl groups of cellulose.
The study of the dispersion demonstrated that acetylated cellulose nanofibers formed stable, well-dispersed suspensions in
both acetone and ethanol. The contact angle measurements showed that the surface characteristics of nanofibers were changed
from hydrophilic to more hydrophobic when acetylated. The microscopy study showed that the acetylation caused a swelling of
the kenaf fiber cell wall and that the diameters of isolated nanofibers were between 5 and 50 nm. X-ray analysis showed that
the acetylation process reduced the crystallinity of the fibers, whereas mechanical isolation increased it. The method used
provides a novel processing route for producing cellulose nanofibers with hydrophobic surfaces. 相似文献
6.
A simple method for preparing redispersible nanofibers from sugar beet residue and their use as a well-dispersed reinforcement for a polyvinyl alcohol (PVA) matrix is reported. It is known that the redispersion of dried cellulose nanofibers is difficult because of the formation of strong hydrogen bonds between the nanofibers. The results show that the properties of the initial sugar beet nanofiber suspension can be recovered without the use of chemical modification or additives with higher pectin and hemicellulose content. Undried and redispersed nanofibers with and without pectin were used as nanocomposite reinforcement with PVA. The redispersed nanofibers were as good reinforcements as the undried nanofibers. The tensile strength and elastic modulus of the nanocomposites with the redispersed sugar beet nanofibers were as good as those of the nanocomposites with undried nanofibers. Interestingly, the nanofiber dispersion in the PVA matrix was better when sugar beet nanofibers containing pectin and hemicellulose were used as reinforcements. 相似文献
7.
Heikkinen JJ Kivimäki L Määttä JA Mäkelä I Hakalahti L Takkinen K Kulomaa MS Hytönen VP Hormi OE 《Colloids and surfaces. B, Biointerfaces》2011,87(2):409-414
A bio-ink for covalent deposition of thermostable, high affinity biotin-binding chimeric avidin onto sol-gel substrates was developed. The bio-ink was prepared from heterobifunctional crosslinker 6-maleimidohexanoic acid N-hydroxysuccinimide which was first reacted either with 3-aminopropyltriethoxysilane or 3-aminopropyldimethylethoxysilane to form silane linkers 6-maleimide-N-(3-(triethoxysilyl)propyl)hexanamide or -(ethoxydimethylsilyl)propyl)-hexanamide. C-terminal cysteine genetically engineered to chimeric avidin was reacted with the maleimide group of silane linker in methanol/PBS solution to form a suspension, which was printed on sol-gel modified PMMA film. Different concentrations of chimeric avidin and ratios between silane linkers were tested to find the best properties for the bio-ink to enable gravure or inkjet printing. Bio-ink prepared from 3-aminopropyltriethoxysilane was found to provide the highest amount of active immobilized chimeric avidin. The developed bio-ink was shown to be valuable for automated fabrication of avidin-functionalized polymer films. 相似文献
8.
A. G. Vendilo H. Rönkkömäki M. Hannu-Kuure M. Lajunen Y. Asikkala A. A. Petrov V. G. Krasovsky E. A. Chernikova P. Oksman L. H. J. Lajunen K. I. Popov 《Russian Journal of Coordination Chemistry》2008,34(9):635-640
The stability constants of the complex[Cs(18C6)]+ (18C6 is 18-crown-6 (L)) in N-butylpyridinium methyl sulfate (I) and of the complex [Cs(18C6)2]+ in 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide (II) were measured by using 133Cs NMR spectroscopy at 23°C. It was found that logK(Cs + L) in solvent I is 1.20±0.13 and logK(CsL + L) in solvent IIis 1.18±0.05. For the complex [Cs(18C6)2]+, the dependence of its stability constant on the temperature in the 23–50°C range was obtained and the enthalpy change in the complexation was determined: ΔH(CsL + L)= ?47 kJ/mol. It was demonstrated that the enthalpy change is favorable for the formation of [Cs(18C6)2]+, while the entropy change hinders the complexation. 相似文献
9.
Ch. Eyholzer F. Lopez-Suevos P. Tingaut T. Zimmermann K. Oksman 《Cellulose (London, England)》2010,17(4):793-802
Bionanocomposites of hydroxypropyl cellulose (HPC) and nanofibrillated cellulose (NFC) were prepared by solution casting. The various NFC were in form of powders and were prepared from refined, bleached beech pulp (RBP) by mechanical disintegration, optionally combined with a pre- or post mechanical carboxymethylation. Dynamic mechanical analysis (DMA) and tensile tests were performed to compare the reinforcing effects of the NFC powders to those of their never-dried analogues. For unmodified NFC powders an inferior reinforcing potential in HPC was observed that was ascribed to severe hornification and reagglomeration of NFC. In contrast, the composites with carboxymethylated NFC showed similar behaviors, regardless of the NFC suspensions being dried or not prior to composite preparation. SEM characterization confirmed a homogeneous dispersion of dried, carboxymethylated NFC within the HPC matrix. These results clearly demonstrate that drying of carboxymethylated NFC to a powder does not decrease its reinforcing potential in (bio)nanocomposites. 相似文献
10.
The asymmetric synthesis of a series of (7'S,8R,8'R)-7'-hydroxylignano-9,9'-lactones is presented, among them the mammalian lignan (7'S)-hydroxyenterolactone and (7'S)-parabenzlactone, allowing the stereochemistry of natural occurring (-)-parabenzlactone to be re-assigned. A hydroxylactone rearrangement and its possible mechanisms are discussed. Finally a brief survey of the current naming and numbering variants of 7'-hydroxylignano-9,9'-lactones is presented, along with a suggestion for harmonization of the nomenclature. 相似文献