Krygowski tadeusz (23 risultati)
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Editore: Warszawa: Sport i Turystyka, 1965, 1965
Da: POLIART Beata Kalke, Tworog, PoloniaPOLIART Beata Kalke
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Aggiungi al carrelloOprawa wydawnicza plotno. @ Cover design and illustrations / Projekt okladki i ilustracje: Projekt okladki Tadeusz Babicz; @ Blurb / Notka wydawnicza: Warszawa: Sport i Turystyka, 1965; @ Size of the book block / Wymiar bloku: 18 cm; @ Attachments / Zalaczniki: [1]k. tabl. zloz. mapa.; @ Circulation / Naklad: 20205; @ Weight / W…aga: 190; @ Pages / Strony: 214, [2]s.; @ Thematic categories / Kategorie tematyczne: geografia przewodniki i informatory, ilustratorzy graficy Babicz Tadeusz, regiony rzeszowszczyzna / geography guide-books, , regions / Geografie Führer, , Regionen; Oprawa nieco uszkodzona, blok pekniety, czysty, jedna karta nieznacznie uszkodzona. Pozycja w stanie wiecej niz dobrym. Projekt okladki Tadeusz Babicz (illustratore).
Lingua: Inglese
Editore: Springer Nature, 2020
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Aggiungi al carrelloN.A. Condizione: New. ISBN:9783662598764.
Aromaticity and Antiaromaticity : Basics and Applications
Solà, Miquel; Boldyrev, Alexander I.; Cyrañski, Michal K.; Krygowski, Tadeusz M.; Merino, Gabriel
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Aromaticity and Antiaromaticity: Concepts and Applications
Solagrave;, Miquel; Boldyrev, Alexander I.; Cyrantilde;ski, Michal K.; Krygowski, Tadeusz M.; Merino, Gabriel
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Aromaticity and Antiaromaticity: Concepts and Applications
Solagrave;, Miquel; Boldyrev, Alexander I.; Cyrantilde;ski, Michal K.; Krygowski, Tadeusz M.; Merino, Gabriel
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Aromaticity and Antiaromaticity : Basics and Applications
Solà, Miquel; Boldyrev, Alexander I.; Cyrañski, Michal K.; Krygowski, Tadeusz M.; Merino, Gabriel
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Aromaticity and Antiaromaticity : Basics and Applications
Solà, Miquel; Boldyrev, Alexander I.; Cyrañski, Michal K.; Krygowski, Tadeusz M.; Merino, Gabriel
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Aromaticity and Antiaromaticity : Basics and Applications
Solà, Miquel; Boldyrev, Alexander I.; Cyrañski, Michal K.; Krygowski, Tadeusz M.; Merino, Gabriel
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Da: GreatBookPricesUK, Woodford Green, Regno UnitoGreatBookPricesUK
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Aromaticity and Antiaromaticity: Concepts and Applications
Solagrave;, Miquel; Boldyrev, Alexander I.; Cyrantilde;ski, Michal K.; Krygowski, Tadeusz M.; Merino, Gabriel
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Da: Majestic Books, Hounslow, Regno UnitoMajestic Books
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Da: preigu, Osnabrück, Germaniapreigu
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Taschenbuch. Condizione: Neu. Aromaticity in Heterocyclic Compounds | Tadeusz Marek Krygowski (u. a.) | Taschenbuch | Topics in Heterocyclic Chemistry | xiii | Englisch | 2010 | Springer | EAN 9783642087936 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]spr…inger[dot]com | Anbieter: preigu.
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Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
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Buch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Aromaticity is a notion that appeared in the mid-nineteenth century to differentiate between unsaturated hydrocarbons and formally unsaturated benzene [1-3]. At the end of the nineteenth century it seemed that cyclicity was a necessary condition for diff…erentiation between the two, but at the beginning of the twentieth century it turned out that the above assumption was not correct because cyclooctatetraene exhibited typical properties known for polyenes [4]. The essential property of b- zene-like compounds, often identified with aromatic compounds, was low react- ity. Hence thermodynamic stability was defined as resonance energy [5, 6] and was the first quantitative measure of aromaticity. Many theoretical approaches were proposed later to estimate this quantity, and now the criterion is often considered to be the most fundamental [7]. Almost at the same time, magnetic susceptibility was used to describe aromaticity [8, 9]. Consequently, many concepts based on mag- tism were developed, probably the most effective in assessment of aromaticity being nucleus independent chemical shift (NICS) [10] or Fowler's maps of ring currents [11]. The criterion served Schleyer as a basis for a definition of aromat- ity: 'Compounds which exhibit significantly exalted diamagnetic susceptibility are aromatic. Cyclic delocalisation may also result in bond length equalization, abn- mal chemical shifts and magnetic anisotropies, as well as chemical and physical properties which reflect energetic stabilisation'[12].
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Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH
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Taschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Aromaticity is a notion that appeared in the mid-nineteenth century to differentiate between unsaturated hydrocarbons and formally unsaturated benzene [1-3]. At the end of the nineteenth century it seemed that cyclicity was a necessary condition f…or differentiation between the two, but at the beginning of the twentieth century it turned out that the above assumption was not correct because cyclooctatetraene exhibited typical properties known for polyenes [4]. The essential property of b- zene-like compounds, often identified with aromatic compounds, was low react- ity. Hence thermodynamic stability was defined as resonance energy [5, 6] and was the first quantitative measure of aromaticity. Many theoretical approaches were proposed later to estimate this quantity, and now the criterion is often considered to be the most fundamental [7]. Almost at the same time, magnetic susceptibility was used to describe aromaticity [8, 9]. Consequently, many concepts based on mag- tism were developed, probably the most effective in assessment of aromaticity being nucleus independent chemical shift (NICS) [10] or Fowler's maps of ring currents [11]. The criterion served Schleyer as a basis for a definition of aromat- ity: 'Compounds which exhibit significantly exalted diamagnetic susceptibility are aromatic. Cyclic delocalisation may also result in bond length equalization, abn- mal chemical shifts and magnetic anisotropies, as well as chemical and physical properties which reflect energetic stabilisation'[12].
Aromaticity in Heterocyclic Compounds
Krygowski, Tadeusz Marek (Edited by)/ Cyranski, Michal Ksawery (Edited by)
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Da: Revaluation Books, Exeter, Regno UnitoRevaluation Books
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Da: moluna, Greven, Germaniamoluna
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Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Heterocyclic chemistry is the biggest branch of chemistry covering two-third of the chemical literatureSeries covers hot topics of frontier research summarized by reputed scientists in the field Our review series is…topic relatedOnli.
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Da: moluna, Greven, Germaniamoluna
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Gebunden. Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Heterocyclic chemistry is the biggest branch of chemistry covering two-third of the chemical literatureSeries covers hot topics of frontier research summarized by reputed scientists in the field Our review…series is topic relatedOnli.
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Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.
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Buch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Aromaticity is a notion that appeared in the mid-nineteenth century to differentiate between unsaturated hydrocarbons and formally unsaturated benzene [1-3]. At the end of the nineteenth century it seemed that cyclicity was a necessary co…ndition for differentiation between the two, but at the beginning of the twentieth century it turned out that the above assumption was not correct because cyclooctatetraene exhibited typical properties known for polyenes [4]. The essential property of b- zene-like compounds, often identified with aromatic compounds, was low react- ity. Hence thermodynamic stability was defined as resonance energy [5, 6] and was the first quantitative measure of aromaticity. Many theoretical approaches were proposed later to estimate this quantity, and now the criterion is often considered to be the most fundamental [7]. Almost at the same time, magnetic susceptibility was used to describe aromaticity [8, 9]. Consequently, many concepts based on mag- tism were developed, probably the most effective in assessment of aromaticity being nucleus independent chemical shift (NICS) [10] or Fowler's maps of ring currents [11]. The criterion served Schleyer as a basis for a definition of aromat- ity: 'Compounds which exhibit significantly exalted diamagnetic susceptibility are aromatic. Cyclic delocalisation may also result in bond length equalization, abn- mal chemical shifts and magnetic anisotropies, as well as chemical and physical properties which reflect energetic stabilisation'[12]. 360 pp. Englisch.
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Da: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, GermaniaBuchWeltWeit Ludwig Meier e.K.
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Taschenbuch. Condizione: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Aromaticity is a notion that appeared in the mid-nineteenth century to differentiate between unsaturated hydrocarbons and formally unsaturated benzene [1-3]. At the end of the nineteenth century it seemed that cyclicity was a neces…sary condition for differentiation between the two, but at the beginning of the twentieth century it turned out that the above assumption was not correct because cyclooctatetraene exhibited typical properties known for polyenes [4]. The essential property of b- zene-like compounds, often identified with aromatic compounds, was low react- ity. Hence thermodynamic stability was defined as resonance energy [5, 6] and was the first quantitative measure of aromaticity. Many theoretical approaches were proposed later to estimate this quantity, and now the criterion is often considered to be the most fundamental [7]. Almost at the same time, magnetic susceptibility was used to describe aromaticity [8, 9]. Consequently, many concepts based on mag- tism were developed, probably the most effective in assessment of aromaticity being nucleus independent chemical shift (NICS) [10] or Fowler's maps of ring currents [11]. The criterion served Schleyer as a basis for a definition of aromat- ity: 'Compounds which exhibit significantly exalted diamagnetic susceptibility are aromatic. Cyclic delocalisation may also result in bond length equalization, abn- mal chemical shifts and magnetic anisotropies, as well as chemical and physical properties which reflect energetic stabilisation'[12]. 360 pp. Englisch.
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Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000
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Buch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Aromaticity is a notion that appeared in the mid-nineteenth century to differentiate between unsaturated hydrocarbons and formally unsaturated benzene [1¿3]. At the end of the nineteenth century it seemed that cyclicity was a necessary condit…ion for differentiation between the two, but at the beginning of the twentieth century it turned out that the above assumption was not correct because cyclooctatetraene exhibited typical properties known for polyenes [4]. The essential property of b- zene-like compounds, often identified with aromatic compounds, was low react- ity. Hence thermodynamic stability was defined as resonance energy [5, 6] and was the first quantitative measure of aromaticity. Many theoretical approaches were proposed later to estimate this quantity, and now the criterion is often considered to be the most fundamental [7]. Almost at the same time, magnetic susceptibility was used to describe aromaticity [8, 9]. Consequently, many concepts based on mag- tism were developed, probably the most effective in assessment of aromaticity being nucleus independent chemical shift (NICS) [10] or Fowler¿s maps of ring currents [11]. The criterion served Schleyer as a basis for a definition of aromat- ity: ¿Compounds which exhibit significantly exalted diamagnetic susceptibility are aromatic. Cyclic delocalisation may also result in bond length equalization, abn- mal chemical shifts and magnetic anisotropies, as well as chemical and physical properties which reflect energetic stabilisation¿[12].Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 360 pp. Englisch.
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Da: buchversandmimpf2000, Emtmannsberg, BAYE, Germaniabuchversandmimpf2000
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Taschenbuch. Condizione: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Aromaticity is a notion that appeared in the mid-nineteenth century to differentiate between unsaturated hydrocarbons and formally unsaturated benzene [1¿3]. At the end of the nineteenth century it seemed that cyclicity was a necessary… condition for differentiation between the two, but at the beginning of the twentieth century it turned out that the above assumption was not correct because cyclooctatetraene exhibited typical properties known for polyenes [4]. The essential property of b- zene-like compounds, often identified with aromatic compounds, was low react- ity. Hence thermodynamic stability was defined as resonance energy [5, 6] and was the first quantitative measure of aromaticity. Many theoretical approaches were proposed later to estimate this quantity, and now the criterion is often considered to be the most fundamental [7]. Almost at the same time, magnetic susceptibility was used to describe aromaticity [8, 9]. Consequently, many concepts based on mag- tism were developed, probably the most effective in assessment of aromaticity being nucleus independent chemical shift (NICS) [10] or Fowler¿s maps of ring currents [11]. The criterion served Schleyer as a basis for a definition of aromat- ity: ¿Compounds which exhibit significantly exalted diamagnetic susceptibility are aromatic. Cyclic delocalisation may also result in bond length equalization, abn- mal chemical shifts and magnetic anisotropies, as well as chemical and physical properties which reflect energetic stabilisation¿[12].Springer-Verlag KG, Sachsenplatz 4-6, 1201 Wien 360 pp. Englisch.
