Boronate gel

We also found that boronate affinity gels failed to retain nicotinamide-photolabeled fragment A or its peptides. In contrast, radiolabeled peptides from fragment A irradiated in the presence of phosphate- or adenine-labeled NAD bound quantitatively to such resins and could be eluted at pH 5.0. Since boronate gels bind compounds containing unblocked vicinal hydroxyls, we concluded that neither of the ribosyl moieties of NAD was present (at least in unmodified form) in the nicotinamide-labeled photoproduct. 

Synthesis and purification of 2 dNAD+. We used p-NMN+ adenyl transferase to synthesize [adenylate- P]2 dNAD+ from [a-3 ]2 dATP. Residual 2 dATP was removed by affinity chromatography on a boronate gel as described elsewhere (14). The elimination of contaminating P-NMN+ (Fig. lA), which also boimd to the boronate gel, was facilitated by its conversion to nicotinamide ribose by treatment with bacterial alkaline phosphatase (Fig. IB). Figure 1C shows that following preparative HPLC, a single peak corresponding to pure 2 dNAD was detected. It is important to note that all of the 32p radiolabel co-eluated with this peak. 

J. H. Hageman and G. D. Kuehn, Assay of Adenylate-Cyclase by Use of Polyacrylamide-Boronate Gel Columns, Anal. Biochem., 1977, 80(2),... 

A solution of 6-bromoindole (O.lOmol) in toluene (200 ml) was treated with Pd(PPh3)4 (5mol%) and stirred for 30 min. A solution of 4-fluorophenyl-boronic acid (0.25 M, 0.15 mol) in abs. EtOH was added, followed immediately by sal aq. NaHCOj (10 eq.). The biphasic mixture was refluxed for several hours and then cooled to room temperature. The reaction mixture was poured into sat. aq. NaCl (200 ml) and the layers separated. The aq. layer was extracted with additional EtOAc (200 ml) and the combined organic layers dried (Na2S04), filtered and concentrated in vacuo. The solution was filtered through silica gel using hexane-CHjCl -hexanc for elution and evaporated. Final purification by recrystallization gave the product (19 g, 90%). 

The reaction of adipic acid with ammonia in either Hquid or vapor phase produces adipamide as an intermediate which is subsequentiy dehydrated to adiponitrile. The most widely used catalysts are based on phosphoms-containing compounds, but boron compounds and siHca gel also have been patented for this use (52—56). Vapor-phase processes involve the use of fixed catalyst beds whereas, in Hquid—gas processes, the catalyst is added to the feed. The reaction temperature of the Hquid-phase processes is ca 300°C and most vapor-phase processes mn at 350—400°C. Both operate at atmospheric pressure. Yields of adipic acid to adiponitrile are as high as 95% (57). 

Inorganic Esters. Boric acid and borax form cycHc esters with poly(vinyl alcohol) (85—100). The reaction is markedly sensitive to pH, boric acid concentration, and the cation-to-boron ratio. An insoluble gel is formed at pH above 4.5—5.0 ... 

The vapor-phase esterification of ethanol has also been studied extensively (363,364), but it is not used commercially. The reaction can be catalyzed by siUca gel (365,366), thoria on siUca or alumina (367), zirconium dioxide (368), and by xerogels and aerogels (369). Above 300°C the dehydration of ethanol becomes appreciable. Ethyl acetate can also be produced from acetaldehyde by the Tischenko reaction (370—372) using an aluminum alkoxide catalyst and, with some difficulty, by the boron trifluoride-catalyzed direct esterification of ethylene with organic acids (373). 

The oligomerization of cardanol with boron trifluoride etharate as the initiator was studied in detail by Antony et al. [171]. The reaction conditions were optimized by using gel permeation chromatography as 140°C with an initiator concentration of 1%. GPC data indicate conversion of all monoene, diene, and triene components into polymer except the saturated component, indicating participation of all the unsaturated components in polymerization. It is possible that the initiation of po-... 

In situ densitometry has been the most preferred method for quantitative analysis of substances. The important applications of densitometry in inorganic PLC include the determination of boron in water and soil samples [38], N03 and FefCNfg in molasses [56], Se in food and biological samples [28,30], rare earths in lanthanum, glass, and monazite sand [22], Mg in aluminum alloys [57], metallic complexes in ground water and electroplating waste water [58], and the bromate ion in bread [59]. TLC in combination with in situ fluorometry has been used for the isolation and determination of zirconium in bauxite and almnimun alloys [34]. The chromatographic system was silica gel as the stationary phase and butanol + methanol + HCl -H water -n HF (30 15 30 10 7) as the mobile phase. 

The medicinal chemists subsequently discovered an improved route to racemic acid 9 that started with 2-bromo-2-cyclopente-l-one 11 (Scheme 7.2) [5]. Suzuki-Miyaura cross-coupling of 11 with 4-fluorophenyl boronic acid 12 provided 13 in 67% yield. Conjugate addition of cyanide furnished ketone 14 in 71% yield. Reduction of 14 with NaB H4 gave a 2.8 1 mixture of desired 15 and undesired 16 which were separated by silica gel chromatography. The observed diastereoselec-tivity with the cyano group was similar to ester 6. Hydrolysis of 15 with 5 M NaOH in MeOH gave racemic acid 9 in 91% yield, which was resolved as outlined in Scheme 7.1. 

Although a number of factors affect structural evolution in sol-gel processing, many of the observed trends can be explained on the basis of the stability of the M-O-M bond in its synthesis environment. Structures which form in solution are the products of a successive series of hydrolysis, condensation and restructuring reactions. M-0-M bonds which are unstable with respect to hydrolysis and alcoholysis are absent. In borates this criterion precludes gelation for systems with insufficient fractions of 4-coordinated borons. In silicates... 

There is great interest in developing molecular precursors for boron-nitrogen polymers and boron nitride solid state materials, and one general procedure is described in this report. Combinations of B-trichloroborazene and hexamethyldisilazane lead to formation of a gel which, upon thermolysis, gives hexagonal boron nitride. The BN has been characterized by infrared spectroscopy, x-ray powder diffraction and transmission electron microscopy. 

A colorless gel formed which was isolated by vacuum evaporation of the volatiles. The resulting colorless glassy solid was pyrolyzed in vacuo at 900°C for 24 hours in a quartz tube and the evolved volatiles identified as NH3 and NH4CI. The remaining solid was briefly (2 hours) heated in air at 1200°C in order to remove minor carbon impurities and to improve crystallinity. This solid was then treated at room temperature with 40% aqueous HF to remove boric acid and silica formed in small quantities. The solid obtained at 900°C was identified as boron nitride however, the majority of the material was amorphous. After treatment at 1200°C, white crystalline boron-nitride was obtained in about 55% yield. 

The use of other crosslinking metals developed simultaneously with the use of antimony, chromium, and boron(borate). Tiner, et al.(242) introduced titanium (IV) crosslinkers in 1975 as ammonium tetralactonate or bis(triethanolamine)bis(isopropyl)titanium(IV). Upon contact with water soluble titanium (IV) derivatives ordinarily form orthotitanic acid, Ti(0H)4, which rapidly forms oligimeric metatitanic acid, [Ti(0H)2] and titanium dioxide. Electron donors such as the hydroxyl groupsxof polysaccharides, if properly oriented, can participate in the sequence of titania reactions and a crosslinked gel network results. Various titanium metal crosslinkers remain in common use today. More will be said about titanium crosslinked gels later. 

Conjugated boron polymers containing platimnn or palladium atom in the main chain were also prepared by hydroboration polymerization between tetrayne/ metal complex monomers and tripylborane (scheme 16).30 From gel permeation chromatographic analysis [THF, polystyrene (PSt) standards], the number-average molecular weights of the polymers obtained were found to be 9000. The polymers were soluble in common organic solvents such as THF, chloroform, and benzene. The absorption peaks due to tt-tt transition were observed around 390 nm in the UV-vis spectra of these polymers. The fluorescence emission spectra exhibited intense peaks at 490 nm in chloroform. 

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