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  • Inorganic Chemistry  (5)
  • germacranolides  (4)
  • rice yield  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 21 (1982), S. 157-160 
    ISSN: 0031-9422
    Keywords: Compositae ; Inula cuspidata ; acetylenic sulfoxides. ; germacranolides ; hydroxygermacrene ; sesquiterpene lactones
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 21 (1982), S. 2029-2033 
    ISSN: 0031-9422
    Keywords: Compositae ; D. anomala subsp. cirsioides ; D. macrocephala ; D. schinzii ; D. zeyheri ; Dicoma anomala subsp. anomala ; Mutisieae ; acetylenic compounds. ; eudesmanolide ; germacranolides ; guaianolide ; sesquiterpene lactones
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 21 (1982), S. 2122-2124 
    ISSN: 0031-9422
    Keywords: Compositae ; Dicoma tomentosa ; Mutisieae ; germacranolides ; melampolides. ; sesquiterpene lactones
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 24 (1985), S. 2023-2028 
    ISSN: 0031-9422
    Keywords: Blainvillea acmella ; Compositae ; acanthospermolides. ; germacranolides ; melampolides ; ovatifolin derivatives ; sesquiterpene lactones
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Plant and soil 102 (1987), S. 41-47 
    ISSN: 1573-5036
    Keywords: Azolla pinnata ; dual cropping ; N2-fixation ; spacing ; rice yield
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A field experiment conducted at Central Rice Research Institute, Cuttack, during three successive seasons showed that with the 120-day-duration variety Ratna two dual crops ofAzolla pinnata R. Brown (Bangkok isolate) could be achieved 25 and 50 days after transplanting (DAT) by inoculating 2.0 t ha−1 of fresh Azolla 10 and 30 DAT respectively. One basal crop of Azolla could also be grown using the same inoculum 20 days before transplanting (DBT) in fallow rice fields. The three crops of Azolla grown—once before transplanting and twice after transplanting—gave an average total biomass of 38–63 and 43–64 t ha−1 fresh Azolla containing 64–90 and 76–94 kg N ha−1 respectively in the square and rectangular spacings. Two crops of Azolla grown only as a dual crop, on the other hand, gave 26–39 and 29–41 t ha−1 fresh Azolla which contained 44–61 and 43–59 kg N ha−1 respectively. Growth and yield of rice were significantly higher in Azolla basal plus Azolla dual twice incorporated treatments than in the Azolla dual twice incorporation, Azolla basal plus 30 kg N ha−1 urea and 60 kg N ha−1 urea treatments. Azolla basal plus 30 kg N ha−1 urea and 60 kg N ha−1 urea showed similar yields but Azolla dual twice incorporation was significantly lower than those. The different spacing with same plant populations did not affect growth and yield significantly, whereas Azolla growth during dual cropping was 8.3 and 64% more in the rectangular spacing than in the square spacing in Azolla basal plus Azolla dual twice incorporation and Azolla dual twice incorporation treatments.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1573-5036
    Keywords: Azolla caroliniana ; Azolla pinnata ; nitrogen fixation ; Oryza sativa ; phosphate fertilizer ; rice yield
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The response of rice toAzolla caroliniana, newly introduced in India, was compared with the reponse to the local isolate ofAzolla pinnata at varying rates of phosphate fertilizer (4.4–8.8 kg P ha−1) during a wet and a dry season. Fresh weight, dry weight and fixed N were more for both species 21 DAI (days after inoculation) than 14 DAI, but acetylene reduction activity (ARA) was higher 14 DAI than 21 DAI. Dry weight of Azolla and fixed N were less 14 DAI forA. caroliniana than forA. pinnata during the wet season. Twenty-one DAI, fresh weight ofA. caroliniana was 62.1 and 27.6% higher than that ofA. pinnata during the wet and dry season, respectively. However, dry weight and fixed N were more 21 DAI inA. caroliniana than inA. pinnata during only the wet season. The ARA was higher inA. caroliniana both 14 and 21 DAI, irrespective of season. The presence of either species in the rice field increased grain yield, straw yield, number of panicles m−2, number of grains per panicle and reduced percentage sterility during both the wet and the dry season. Phosphate application significantly increased fresh weight, dry weight, ARA and fixed N for both species as well as grain and straw yields of rice. The responses to phosphate fertilizer were similar for both Azolla species and for rice grown with either one of the Azolla species.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1573-0867
    Keywords: Azolla caroliniana ; N2-fixation ; rice yield ; crop N uptake
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Experiment with different split applications of 40 kg N ha−1 of urea (U) at transplanting:30 days after transplanting:40 days before crop maturity with different proportions of 50:25:25, 25:50:25 and 0:50:50 splits, with and without Azolla, carried out for two consecutive seasons, revealed that fresh weight (FW), N2-fixation measured by acetylene reduction activity (ARA) and N yield of newly introducedAzolla caroliniana were higher with 0:50:50 treatment followed by 25:50:25 and 50:25:25.Azolla was unincorporated and left for self decomposition. The crop yield (grain yield, straw yield) and crop N uptake data indicated that among the no Azolla treatments, the use of 50:25:25 split resulted in highest crop yield and crop N uptake followed by 25:50:25 and 0:50:50 treatments, while these parameters recorded maximum value with 25:50:25 split in combination with Azolla followed by 50:25:25 and 0:50:50 treatments. The use of Azolla increased crop yield and crop N uptake significantly over no Azolla treatments.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 1093-1098 
    ISSN: 0009-2940
    Keywords: Indium tris(thiobenzoate) ; Triethylammonium tetrakis(thiobenzoato)indate ; Tin, butyl-, tris(thiobenzoate) ; Tin, dichloro-, bis(thiobenzoate) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Indium(III) and tin(IV) thiocarboxylates were prepared and characterized on the basis of their IR, 13C- and 19Sn-NMR data. Indium tris(thiobenzoate) (1) decomposes into a sulfido complex In (S)[S(O)CPh] (2a). The corresponding tris(thioacetate) In[S(O)CMe]3 is thermally too unstable to be isolated. The anionic tetrakis complex [Et3NH]{In[S(O)CPh]4} (3) was characterized by X-ray crystallography which revealed a distorted tetrahedral coordination at the In atom. X-ray diffraction analysis of the complexes BuSn[S(O)CPh]3 (4) and Cl2Sn[S(O)CPh]2 (7) showed distorted tetrahedral and cis-octahedral structures, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 332 (1964), S. 103-112 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Darstellung und Eigenschaften von Additionsverbindungen des SnCl4 mit N, N-Dimethylformamid, Acetamid, Acetanilid und Benzamid werden mitgeteilt. Neben der Analyse zeigen auch Donator-Acceptor-Titrationen in Dichloräthan die allgemeine Formel SnCl4 · 2 Amid. Leitfähigkeitsmessungen in Nitromethan und Molekulargewichtsbestimmungen lassen auf das Vorliegen von monomeren Additionsverbindungen schließen. Aus den IR-Spektren geht an Hand einer Erniedrigung der (C—O)- und einer Erhöhung der (C—N)-Valenzschwingung eine Bindung der organischen Liganden an das Zinn über Sauerstoff hervor. Die relativen Basenstärken nehmen in der Reihe Dimethylformamid, Benzamid, Acetanilid, Acetamid ab.
    Notes: The molecular addition compounds of tin (iv) chloride with N, N-dimethyl formamide, acetamide, acetanilide, and benzamide have been prepared. They are of the type SnCl4 · 2 amide. This composition type has been confirmed by indicator titrations of stannic chloride against amides in dichloroethane. Conductivity measurements in nitromethane and molecular weight determinations show that they are true molecular addition compounds being monomeric.The infrared spectra of the adducts show that there are metal-to-oxygen bonds in all these compounds as is evidenced by a negative shift of the carbonyl stretching frequency and a positive shift of the C—N stretching frequency. The relative donor ability of the amides towards stannic chloride has been found to be: dimethyl formamide 〉 benzamide 〉 acetanilide 〉 acetamide.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 423 (1976), S. 173-179 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Untersuchungen an MM″ (NCS)4-Komplexen (M = NiII, FeII, ZnII; M″ = HgII, ZnII)Komplexe des Typs MM′(NCS)4 · xL M = NiII, FeII, ZnII; M″ = HgII, ZnII; x = 2, 4, 6; L = Nicotinamid (nia), Isonicotinsaiurehydroxid (inh) 2-Aminopyrimidin (2apm)] wurden dargestellt und charakterisiert durch Elementaranalyse, molare Leitfähigkeit, magnetisches Moment, IR- und Elektronenspektren.
    Notes: Coordination complexes of the type MM″(NCS)4 · xL M = Ni(II), Fe(II), Zn(II), M″ = Hg(II), Zn(II), x = 2, 4, 6 and L = nicotinamide (nia), 3-cyanopyridine (3-cpy), 4-cyanopyridine (4cpy), 4-aminopyridine (4apy), isonicotinic acid hydrazide (inh), 2-aminopyrimidine (2apm)l have been prepared and characterized by elemental analysis, molar conductance, magnetic moment, infrared and electronic spectral studies. Molar conductance data of NiZn(NCS), complexes are equivalent to 1:1 electrolyte. The infrared spectral studies indicate that only bridged thiocyanate groups are present in the complexes of the type NiHg(SCN)4 · 4L [L=3 and 4cpy, inh] and FeHg(SCN)4 · 2L [L = nia, 2apm], whereas both bridged and terminal thiocyanates are present in the complexes of the type NiHg(SCN)4 · 4L [L = nia, 3apy and ZnHg(SCN)4 · 2(inh). BOHR magneton values and electronic spectral data indicate an octahedral environment around nickel and iron in their complexes. Symmetry and group theory have also been used to establish the structure of the complexes.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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