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Lower Yields (lower + yield)
Selected AbstractsUse of stomatal conductance and pre-dawn water potential to classify terroir for the grape variety KékfrankosAUSTRALIAN JOURNAL OF GRAPE AND WINE RESEARCH, Issue 1 2009Zs. ZSÓFI Abstract Background and Aims:, A 3-year study was carried out in order to evaluate the ecophysiology, yield and quality characteristics of Vitis vinifera L. cv. Kékfrankos (syn. Limberger) at Eger-Nagyeged hill (steep slope) and at Eger-K,lyuktet, (flat) vineyard sites located in the Eger wine region, Hungary. The aim of this paper was to analyse the effect of ,vintage' and ,terroir' on the seasonal changes of Kékfrankos ecophysiology and its possible relationship with yield and wine composition. Methods and Results:, Grapevine physiological responses (midday- and pre-dawn water potential, pressure,volume analysis and gas-exchange), growing stages, yield and wine composition of each vineyard were studied. Lower grapevine water supply was detected at Eger-Nagyeged hill in each season due to its steep slope and soil characteristics. Pressure-volume curves indicated that there was no osmotic adjustment in the leaves of this variety. Higher osmotic concentration was measured at turgor loss and full turgor in the leaves of the unstressed vineyard (Eger-K,lyuktet,) presumably due to higher photosynthetic activity. Differences in soil water content of the vineyards resulted in a slightly altered cell wall elasticity. Stomatal conductance, transpiration rate and photosynthetic production per unit leaf area were affected by water availability. Lower yield in Eger-Nagyeged hill was partly associated with decreased photosynthetic production of the canopy. Improved wine quality of Eger-Nagyeged hill was due to moderate water stress which induced higher concentration of anthocyanins and phenolics in the berries. The duration of the phenological stages was dependent on vintage temperature characteristics rather than on vineyard site. Conclusion:, There was a close relationship between environmental conditions, Kékfrankos gas-exchange, water relations, yield and wine composition. Water deficit plays an important role in creating a terroir effect, resulting in decreased yield, better sun exposure of leaves and clusters and thus higher concentration of phenolics and anthocyanins. Although quality is mainly influenced by vintage differences, vineyard characteristics are able to buffer unfavourable vintage effects even within a small wine region. Significance of the Study:, Stomatal conductance, pre-dawn water potential and climatic data may be reliable parameters for terroir classification, although variety,terroir interactions must always be considered. [source] The Synthesis and Characterisation of Bis(phosphane)-Linked (6 - p -Cymene)ruthenium(II),Borane CompoundsEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 23 2005Adrian B. Chaplin Abstract The reaction of [(,6 - p -cymene)RuCl2]2 with some bis(phosphane) ligands (dppm, dppe, dppv, dppa, dpp14b, dppf) has been investigated. In general mixtures of products were obtained, although the pendant phosphane complexes [(,6 - p -cymene)RuCl2(,1 -dppv)] and [(,6 - p -cymene)RuCl2(,1 -dppa)] were isolated and characterized in the solid state by X-ray diffraction. The later complex was obtained in lower yield and undergoes an equilibration reaction resulting in the formation of a dimeric species, where the dppa bridges two ruthenium centres, and uncoordinated phosphane; the bridging species was also structurally characterised in the solid state. In contrast, the reaction of [(,6 - p -cymene)RuCl2(PPh3)] with dppa in the presence of [NH4]PF6 results in the formation of [(,6 - p -cymene)RuCl(PPh3)(,1 -dppa)]PF6, which is stable in solution. A series of linked ruthenium,borane complexes, viz. [(,6 - p -cymene)RuCl2(,1 -phosphane-BH3)] (phosphane = dppm, dppe, dppv, dppa, dpp14b, dppf) and [(,6 - p -cymene)RuCl(PPh3)(,1 -dppa-BH3)]PF6 have been prepared from isolated pendant phosphane complexes, those generated in situ, or from a preformed phosphane,borane adduct. The solid-state structures of [(,6 - p -cymene)RuCl2(,1 -dppm-BH3)], [(,6 - p -cymene)RuCl2(,1 -dppe-BH3)] and [(,6 - p -cymene)RuCl2(,1 -dppv-BH3)] have been determined by X-ray diffraction analysis. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) [source] A new and simple method for rapid extraction and isolation of high-quality RNA from grape (Vitis vinifera) berriesJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 2 2008Francesca Fort Abstract BACKGROUND: A fast and easy method to isolate RNA from grape (Vitis vinifera) berries is proposed. RESULTS: The procedure uses high concentrations of cetyltrimethylammonium bromide (CTAB) and includes boric acid with the purpose of increasing the RNA extraction. Eppendorf tubes can be used since the amount of sample and volumes of reagents needed are small. The method is based on genomic DNA digestion with DNase I, which avoids the disadvantages of using LiCl (e.g. possible amplification of rare transcripts and reduction or even suppression of the activity of RNA-dependent DNA polymerase). The use of DNase reduces the duration of the isolation method to 8 h. The RNA yield (32.9,49.2 µg g,1) and purity indices were satisfactory in all cases. CONCLUSION: Although there is a referenced grape berry method (RNeasy Midi Kit + polyethylene glycol) that is faster than the one proposed, it is 3.7 times more expensive and gives a lower yield. The ability to successfully amplify from the RNA extract was verified by measuring the ,-tubulin and lipoxygenase gene expression. Copyright © 2007 Society of Chemical Industry [source] Effects of Hordeum chilense cytoplasm on agronomic traits in common wheatPLANT BREEDING, Issue 1 2007S. G. Atienza Abstract The genome of bread wheat, AABBDD, was substituted into the cytoplasm of Hordeum chilense by repeated backcrossing to produce alloplasmic lines. The aim of this work was to investigate the effect of H. chilense cytoplasm on agronomic traits in common wheat. Three cytolines were developed. The alloplasmic nature of these lines was confirmed using chloroplast simple-sequence repeat markers. Each cytoline was compared with its respective euplasmic control for agronomic performance during 2 years of field trials. The interaction between H. chilense cytoplasm and common wheat genome greatly affected most of the traits evaluated. Among them, alloplasmic lines showed delayed anthesis date, lower yield and lower plant height. These effects are similar to those caused by Aegilops cytoplasm. The main conclusion of this work is that H. chilense cytoplasm is of limited value for wheat breeding. [source] Effect of an automatic milking system on milking traitsANIMAL SCIENCE JOURNAL, Issue 5 2002Takashi HAYASHI ABSTRACT Recent studies in Japan of the effect of automatic milking systems (AMS) on the behavior of dairy cows have confirmed the labor-saving aspect of AMS, but have not solved some of the problems affecting milking traits. The influence of AMS on milking was examined in 39 Holstein cows at Iwate Agricultural Research Center from June 1998 to December 1999, by measuring and recording the yield per milking, milking finish time, milking frequency, and daily yield of milking. Four milking traits were analyzed separately as the objective variable in a linear model, with parity, days in milking, month after installation of the AMS as independent variables. Primiparous cows milked more frequently in the middle and late stage of lactation, yielded less per milking and less per day in the early stage of lactation than multiparous cows with the AMS. Lower frequencies were observed at noon and midnight for cleaning of the bulk tank. By contrast, higher milking frequency in the forenoon was shown. The yield per milking rose and declined, following a normal lactation curve. However, milking frequency rose slowly, and declined gradually in the late stage of lactation. After installing a one-way gate, the cows milked more frequently, with a lower yield per milking and a greater daily milk yield, than before installation. [source] Effect of Different Carbon Sources on the Production of Succinic Acid Using Metabolically Engineered Escherichia coliBIOTECHNOLOGY PROGRESS, Issue 2 2007Christian Andersson Succinic acid (SA) is an important platform molecule in the synthesis of a number of commodity and specialty chemicals. In the present work, dual-phase batch fermentations with the E. coli strain AFP184 were performed using a medium suited for large-scale industrial production of SA. The ability of the strain to ferment different sugars was investigated. The sugars studied were sucrose, glucose, fructose, xylose, and equal mixtures of glucose and fructose and glucose and xylose at a total initial sugar concentration of 100 g L,1. AFP184 was able to utilize all sugars and sugar combinations except sucrose for biomass generation and succinate production. For sucrose as a substrate no succinic acid was produced and none of the sucrose was metabolized. The succinic acid yield from glucose (0.83 g succinic acid per gram glucose consumed anaerobically) was higher than the yield from fructose (0.66 g g,1). When using xylose as a carbon source, a yield of 0.50 g g,1 was obtained. In the mixed-sugar fermentations no catabolite repression was detected. Mixtures of glucose and xylose resulted in higher yields (0.60 g g,1) than use of xylose alone. Fermenting glucose mixed with fructose gave a lower yield (0.58 g g,1) than fructose used as the sole carbon source. The reason is an increased pyruvate production. The pyruvate concentration decreased later in the fermentation. Final succinic acid concentrations were in the range of 25,40 g L,1. Acetic and pyruvic acid were the only other products detected and accumulated to concentrations of 2.7,6.7 and 0,2.7 g L,1. Production of succinic acid decreased when organic acid concentrations reached approximately 30 g L,1. This study demonstrates that E. coli strain AFP184 is able to produce succinic acid in a low cost medium from a variety of sugars with only small amounts of byproducts formed. [source] Photoreactivity and Photopolymerization of Silicon-Bridged [1]Ferrocenophanes in the Presence of Terpyridine Initiators: Unprecedented Cleavage of Both Iron,Cyclopentadienyl Bonds in the Presence of ChlorosilanesCHEMISTRY - A EUROPEAN JOURNAL, Issue 31 2007Yan Chan Abstract The photopolymerisation of sila[1]ferrocenophane [Fe(,-C5H4)2SiMe2] (3) with 4,4,,4,,-tri- tert -butyl-2,2,:6,,2,,-terpyridine (tBu3terpy) as initiator has been explored. High-molecular-weight polyferrocenylsilane (PFS) [{Fe(,-C5H4)2SiMe2}n] (5) was formed in high yield when a stoichiometric amount of tBu3terpy was used at 5,°C. Photopolymerisation of ferrocenophane 3 at higher temperatures gave PFS 5 in lower yield and with a reduced molecular weight as a result of a slower propagation rate. Remarkably, when Me3SiCl was added as a capping agent before photopolymerisation, subsequent photolysis of the reaction mixture resulted in the unprecedented cleavage of both iron,Cp bonds in ferrocenophane 3: iron(II) complex [Fe(tBu3terpy)2Cl2] (7Cl) was formed and the silane fragment (C5H4SiMe3)2SiMe2 (8) was released. The iron,Cp bond cleavage reaction also proceeded in ambient light, although longer reaction times were required. In addition, the unexpected cleavage chemistry in the presence of Me3SiCl was found to be applicable to other photoactive ferrocenes such as benzoylferrocene. For benzoylferrocene and ferrocenophane 3, the presence of metal-to-ligand charge transfer (MLCT) character in their low-energy transitions in the visible region probably facilitates photolytic iron,Cp bond cleavage, but this reactivity is suppressed when the strength of the iron,Cp bond is increased by the presence of electron-donating substituents on the cyclopentadienyl rings. [source] Facile Construction of Spirocyclopropanated Bi-, Tri- and Tetracyclic Skeletons by Novel Cascades Involving Intra- and Intermolecular Heck Reactions of 2-Bromo-1,6-enynes and BicyclopropylideneEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 3 2005Michael Schelper Abstract Acyclic 2-bromo-1,6-enynes 5 -R, 9 -R and 11 -R with bulky substituents at the acetylenic terminus were co-cyclized with the highly strained bicyclopropylidene (12) under palladium catalysis at 80 °C to give the cross-conjugated tetraenes 13 -R, 18 -R and 19 -R in moderate-to-good yields (34,71%). Only the co-cyclization of 5 -Ph gave rise to an additional product, which was identified as the 11-membered ring 20. At elevated temperatures (120,140 °C) the initially formed tetraenes underwent 6,-electrocyclization to give spiro[cyclopropane-1,4,-bicylo[4.3.0]-1(6),2-dienes] 21 -R, 22 -R and 23 -R. This novel class of spirocyclopropanated oligocycles is also accessible by a one-pot protocol. The highest yields for both the tetraenes and bicyclo[4.3.0]nonadiene and its heteroanalogues were obtained with bulky substituents at the alkyne terminus of the precursors. Heteroatom-containing precursors 9 -R and 11 -R gave lower yields than their all-carbon analogues 5 -R. The acyclic 2-bromo-1,8-dien-6-ynes 28a,b,c upon palladium-catalyzed co-cyclization with bicyclopropylidene (12) at 110 °C gave spirocyclopropanated tricycles 31a,b and 32, respectively, in moderate yields (14, 31 and 32%). These products were formed by two consecutive 6,-electrocyclizations. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) [source] Agronomic factors affecting the yield and quality of forage maize in Ireland: effect of sowing date and plastic film treatmentGRASS & FORAGE SCIENCE, Issue 1 2002G. P. Keane The objectives of these studies were to examine the effects of sowing date and plastic film on the yield and quality of forage maize (Zea mays L.) in Ireland, a marginal maize-growing area. In 1989,95, comparisons were made of maize sown through clear plastic film (PP treatment), and maize sown in the conventional manner without plastic (NP treatment), in terms of dry-matter (DM) yield and quality (cob, grain and starch contents). The PP treatment significantly increased DM yields in five years, with a mean yield increase of 3·10 t ha,1. Whole-plant DM content increased (significant in four years) by a mean of 0·15; cob content increased (significant in five years) by a mean of 0·32; grain content increased (significant in all of the three years examined) by 0·75; and starch content increased from 236 to 318 g kg,1 DM (P < 0·01) in 1995 where the plastic film treatment was used. Organic matter digestibility values were similar for both treatments in 1995. Sowing date in the April-May period had no consistent effect on DM yields, but early sowings did increase cob (significant, except in 1994), grain (significant in one (1995) of the two years tested) and starch (P < 0·05) contents (only tested in 1995). Sowing on 11 April 1995 through perforated plastic gave lower yields than the NP treatment sown on the same date, due to severe frost damage in early May. [source] Straw bed priming enhances the methane yield and speeds up the start-up of single-stage, high-solids anaerobic reactors treating plant biomassJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 11 2006L Mattias Svensson Abstract A simple and potentially inexpensive implementation of a high-solids reactor is a single-stage, stratified bed reactor, in which the bed is made up of the plant biomass fed into the system. In the present study, the stratified bed was started up for a period of four weeks by either direct feeding of sugar beet leaves at four different feeding rates, or by introducing a straw bed primer which was batch digested without feeding. During weeks five to six both systems were fed with sugar beet leaves at such a rate that the total amount of beet leaves added at the end of week six was the same in each of the four corresponding pairs of straw and ,no-straw' reactors. Straw bed priming enhanced the methane yield of the sugar beet leaves, with 0.33,0.37 m3 kg,1 VSadded (volatile solids) accumulated at average solid retention times as short as 11,25 days, while the ,no-straw' reactors had lower yields at longer average solid retention times. The levels and speciation of the organic acids suggested that both the rate and extent of the anaerobic digestion of the sugar beet leaves added in the straw reactors were improved. At the highest loading rate, the straw reactor failed, while the ,no-straw' reactor did not. It is hypothesised that the microbial biomass was better established in the straw reactors than in the ,no-straw' reactors. Copyright © 2006 Society of Chemical Industry [source] Microwave-assisted synthesis of new regioisomeric 6,7-dihydroindeno[1,2- e]pyrimido[4,5- b][1,4]diazepin-5(5aH)-onesJOURNAL OF HETEROCYCLIC CHEMISTRY, Issue 6 2008Braulio Insuasty Novel 11-amino-6-aryl-6,7-dihydroindeno[1,2- e] pyrimido[4,5- b][1,4]diazepin-5(5aH)-ones 4a-f were prepared regioselectively by the tricomponent reaction of 4,5,6-triaminopyrimidine 1, 1,3-indandione 2 and aromatic aldehydes 3a-f. The bicomponent approach, using 2,4,5,6-tetraaminopyrimidine 5 and 2-aryl-ideneindandiones 6a-f as reagents, afforded 9,11-diamino-6-aryl-6,7-dihydroindeno[1,2- e]pyrimido[4,5- b]-[1,4]diazepin-5(5aH)-ones 7a-f in good yields and the regioisomeric 8,10-diamino derivatives 8a-c in lower yields. Both, bi- and tricomponent approaches were performed by microwave irradiation and all products were fully characterized by detailed NMR measurements. [source] The Ozone Component of Global Change: Potential Effects on Agricultural and Horticultural Plant Yield, Product Quality and Interactions with Invasive SpeciesJOURNAL OF INTEGRATIVE PLANT BIOLOGY, Issue 4 2009Fitzgerald Booker The productivity, product quality and competitive ability of important agricultural and horticultural plants in many regions of the world may be adversely affected by current and anticipated concentrations of ground-level ozone (O3). Exposure to elevated O3 typically results in suppressed photosynthesis, accelerated senescence, decreased growth and lower yields. Various approaches used to evaluate O3 effects generally concur that current yield losses range from 5% to 15% among sensitive plants. There is, however, considerable genetic variability in plant responses to O3. To illustrate this, we show that ambient O3 concentrations in the eastern United States cause substantially different levels of damage to otherwise similar snap bean cultivars. Largely undesirable effects of O3 can also occur in seed and fruit chemistry as well as in forage nutritive value, with consequences for animal production. Ozone may alter herbicide efficacy and foster establishment of some invasive species. We conclude that current and projected levels of O3 in many regions worldwide are toxic to sensitive plants of agricultural and horticultural significance. Plant breeding that incorporates O3 sensitivity into selection strategies will be increasingly necessary to achieve sustainable production with changing atmospheric composition, while reductions in O3 precursor emissions will likely benefit world food production and reduce atmospheric concentrations of an important greenhouse gas. [source] Alkyl halides reactions with cathodes or with magnesium.JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, Issue 12 2006Grignard reagent studied with radical clocks. Abstract In the mechanism of reaction of Grignard reagent formation for alkyl halides (RX), it is generally assumed that the alkyl radical, formed by the electron transfer from the metal to this halide, reacts rapidly with the paramagnetic MgX, species. The previous comparisons of aryl halides reactivity toward magnesium and their reactivity toward a cathode strongly suggested that MgX, species are not, for the aryl halides, compulsory to rationalise the observed facts. The aryl radicals formed by electron transfer from the metal to the aryl halide would undergo a rapid second electron transfer to yield carbanions transformed into RMgX by reaction with MgX2. In contrast, for the alkyl halides, the reduction of the rapidly formed alkyl radicals into carbanions has seldom been discussed as a possible fate for these radicals, the main discussed fates being dimerisation, disproportionation, hydrogen abstraction from the solvent, rearrangement or coupling with MgX, radicals. Two main differences distinguish the reactivity of alkyl halides from their aryl halides counterpart. First, the radical anions of aryl halides may have a given lifetime whereas electron transfer to alkyl halides is concerted with the cleavage of the molecule. Second, the aryl radicals display far stronger oxidising properties than the alkyl radicals. The counterpart of this property is that aryl carbanions display weaker reducing properties than the alkyl ones. In this report, putting in perspective Grignard reaction and the experimental results obtained with identical radical clocks in electrochemistry, we tentatively provide an answer to the question raised in the title. The comparison of electrochemical patterns of reactivity of selected alkyl halides and the evolutions of yields in the preparation of Grignard reagent suggest a new explanation for the lower yields generally observed when alkyl iodides are the starting substrates. It involves an autocatalytic reaction where carbanionic species formed from the alkyl radicals and diffusing away from the metal surface, transfer one electron to the alkyl halide; the result would be the creation of two radicals leading to an increased amount of by-products. If the carbanionic mechanism were to be retained for the formation of alkyl Grignard reagent one would have to admit that the magnesium surface behaves as a cathode displaying high current densities reminiscent of microelectrodes. Copyright © 2006 John Wiley & Sons, Ltd. [source] Reduction of Botrytis cinerea sporulation in sweet basil by altering the concentrations of nitrogen and calcium in the irrigation solutionPLANT PATHOLOGY, Issue 4 2006U. Yermiyahu Current measures for suppressing grey mould (Botrytis cinerea) on sweet basil rely on fungicide applications and climate control. In this study, the nitrogen and calcium concentrations in the standard irrigation solution (7·2 and 1·3 mm, respectively) were varied in a series of experiments conducted in pots and large containers. Treatments differed in the N or Ca concentrations supplied, and effects on host response were determined in detached stem segments, individual plants and plots. Effects of the two elements on grey mould incidence, lesion size and rate of disease progression were erratic and rarely significant, but decreasing the concentration of N and increasing the concentration of Ca in the irrigation solution decreased sporulation of B. cinerea. In some cases, however, altering the standard irrigation solution resulted in significantly lower yields. Analyses of mineral contents in the shoots suggested that yields were not impaired when N content in the shoots was not reduced below 2·9% and Ca content was not raised above 1·3%. These findings were used to compose a modified irrigation solution containing half of the N (3·6 mm) and double of the Ca (2·55 mm) concentrations in the standard irrigation solution. The modified irrigation solution significantly reduced sporulation of B. cinerea without affecting crop yield. [source] Mechanistic limitations in the synthesis of polyesters by lipase-catalyzed ring-opening polymerizationBIOTECHNOLOGY & BIOENGINEERING, Issue 1 2003Anna A. Panova Abstract Lipase-catalyzed polymerization of caprolactone (CL) in toluene with methoxy-poly(ethylene glycol) (MPEG) and water as initiators was characterized in detail for mechanistic insight. 1H NMR analysis of polycaprolactone chains (PCL), dicaprolactone, degree of esterification of MPEG, and fractions of PCL chains initiated by MPEG and water were used to follow the reactions. The data were analyzed with the kinetic scheme involving formation of the acylenzyme and its consequent reaction with MPEG, water, or PCL to yield the MPEG- or water-initiated PCL chains, or increase in PCL length. A limit for MPEG initiator esterification in lipase-catalyzed CL polymerization was observed and was explained by preferential reaction of PCL propagation over MPEG esterification at long reaction times and low MPEG concentrations. Slower monomer conversion in concentrated monomer solutions was explained by decreased partitioning of PCL between the solvent and the enzyme. This effect resulted in inhibition of the lipase by the reaction product, PCL chains, and/or insufficient diffusion of monomer to the enzyme active site. High monomer/initiators ratio in these solutions did not yield longer polymer chains due to decreased monomer conversion and the corresponding decrease in product yields; lower yields were also observed for chain initiation by MPEG and water. A shift in the reaction rate-limiting step from formation of acylenzyme in dilute CL solutions to its deacylation in concentrated CL solutions yielded higher PCL polydispersity due to increased initiation by water. Enhanced intramolecular cyclization was also observed. Endgroup composition of PCL chains was influenced by the concentration of monomer, ratio of initiators (MPEG and water), and reaction time, yielding PCL chains initiated exclusively by MPEG at "infinite reaction times." © 2003 Wiley Periodicals, Inc. Biotechnol Bioeng 84: 103,113, 2003. [source] Towards Supramolecular Fixation of NOX Gases: Encapsulated Reagents for NitrosationCHEMISTRY - A EUROPEAN JOURNAL, Issue 6 2005Yanlong Kang Abstract The use of simple calix[4]arenes for chemical conversion of NO2/N2O4 gases is demonstrated in solution and in the solid state. Upon reacting with these gases, calixarenes 1 encapsulate nitrosonium (NO+) cations within their cavities with the formation of stable calixarene,NO+ complexes 2. These complexes act as encapsulated nitrosating reagents; cavity effects control their reactivity and selectivity. Complexes 2 were effectively used for nitrosation of secondary amides 5, including chiral derivatives. Unique size,shape selectivity was observed, allowing for exclusive nitrosation of less crowded N -Me amides 5,a,e (up to 95,% yields). Bulkier N -Alk (Alk>Me) substrates 5 did not react due to the hindered approach to the encapsulated NO+ reagents. Robust, silica gel based calixarene material 3 was prepared, which reversibly traps NO2/N2O4 with the formation of NO+ -storing silica gel 4. With material 4, similar size,shape selectivity was observed for nitrosation. The N -Me,N -nitroso derivatives 6,d,e were obtained with ,30,% yields, while bulkier amides were nitrosated with much lower yields (<8,%). Enantiomerically pure encapsulating reagent 2,d was tested for nitrosation of racemic amide 5,t, showing modest but reproducible stereoselectivity and ,15,% ee. Given high affinity to NO+ species, which can be generated by a number of NOX gases, these supramolecular reagents and materials may be useful for NOX entrapment and separation in the environment and biomedical areas. [source] | |||||||||||||