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  • 2005-2009  (41)
  • 1960-1964  (20,531)
  • 1920-1924  (7,605)
  • 1890-1899  (12,616)
  • 1850-1859  (4,468)
  • Chemistry  (45,220)
  • Electronic books  (32)
  • ddc:020  (9)
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  • 1
    Publication Date: 2020-12-11
    Description: Vorbemerkung Beim Schreiben dieses Artikels, der auf Veränderungen der Kommunikations- und Publikationstechniken und ihre Bedeutung hinweist, ist uns mehr als je zuvor bewusst geworden, wie beschränkt das Medium Papier ist. Es gibt z. B. keine Hyperlinks, durch die man unmittelbar das Erwähnte erleben oder überprüfen kann. Ein schneller Wechsel vom Wort zum Bild, zum Ton oder Video ist nicht möglich. Wer will schon lange URLs abtippen und Medienbrüche erleiden? Wir haben uns daher entschlossen, eine textidentische Version dieses Artikels mit allen URLs – sie liegt Ihnen hier vor – elektronisch anzubieten und in der für die "Gegenworte" (BBAW) gekürzten Fassung nur durch [URL] anzudeuten, dass der Leser an dieser Stelle einfach in der elektronischen Version einen Klick ins Internet machen sollte. Und damit sind wir bereits mitten im Thema.
    Keywords: ddc:020
    Language: German
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 2
    Publication Date: 2020-12-11
    Description: Zwischen dem Bibliotheksverbund Bayern (BVB) und dem Kooperativen Bibliotheksverbund Berlin-Brandenburg (KOBV) besteht seit Ende 2007 eine Strategische Allianz, die auf zwei Säulen beruht: einer langfristigen Entwicklungspartnerschaft einerseits und der Kooperation im Dienstleistungsbereich mit der Integration der Verbundkataloge andererseits. Ende 2008 wurde das erste Entwicklungsprojekt "Literaturverwaltungsprogramme" abgeschlossen, dessen Ergebnisse in dieser Handreichung in Form von Handlungsempfehlungen für Bibliotheken vorgestellt werden. Ziel des Projekts war es, den Datenaustausch zwischen den Bibliotheks- und Verbundkatalogen des BVB und KOBV und gängigen Literaturverwaltungsprogrammen zu optimieren. Neben Handlungsempfehlungen für die Implementierung neuer Exportschnittstellen und die Verbesserung bestehender Exportmöglichkeiten werden Hinweise auf verbesserte Nutzerführung gegeben. Die Empfehlungen beziehen sich vorwiegend auf den Datenaustausch zwischen den Bibliothekssystemen Aleph 500, MetaLib und WebOPAC/InfoGuide und den Literaturverwaltungsprogrammen Citavi, EndNote, RefWorks und Zotero.
    Keywords: ddc:020
    Language: German
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 3
    Publication Date: 2020-12-11
    Description: Gemeinsame Web-Auftritte zu organisieren, die sich über mehrere Institutionen und Fachgebiete erstrecken, ist eine anspruchsvolle und faszinierende Aufgabe, die auf verschiedene Weise gelingen, aber auch scheitern kann. Wer sich daran versucht, tut gut daran, sich über bestimmte Prinzipien und technische Mittel zu informieren, die das fortgeschrittene Web ihm heute bietet. Das Internet, das World Wide Web und das moderne Web 2.0 sind in einer fast zwanzig Jahre dauernden Kollaboration einer globalen Gemeinschaft von Entwicklern und Anwendern entstanden. Es enthält heute eine Fülle sofort einsetzbarer Komponenten, von der „Benutzerdefinierten Google-Suche Beta“ mit Google‘s PageRanking auf ausgewählten Web-Seiten bis hin zum automatisierten Web-Server mit Content-Management für das „Mitmach-Web“. Der Artikel stellt nur eine kleine Auswahl solcher Lösungen vor und macht den Versuch, einige Prinzipien des Web 2.0 so herauszuarbeiten, dass die notwendige Kommunikation zwischen Managern, Technikern, Redakteuren und Organisatoren in der kleinen Kollaboration unterstützt wird. „Kleine Kollaboration“ bedeutet hier, dass es nicht um die globale Vernetzung von technischen Großgeräten der e-Science gehen soll, auch nicht um die Super-Suchmaschine in Europa, sondern um die Unterstützung der Zusammenarbeit und Kommunikation von Wissenschaftlern und Museumsfachleuten mit Ihren Nutzern.
    Keywords: ddc:020
    Language: German
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 4
    Publication Date: 2024-01-12
    Description: Im Kooperativen Bibliotheksverbund Berlin-Brandenburg (KOBV) wird für die automatisierte Fernleihe der Zentrale-Fernleihserver (ZFL-Server) der Firma Sisis eingesetzt. Die Software ist in der KOBV-Zentrale installiert. Der ZFL-Server dient im KOBV sowohl für die Bestellung von Monographien als auch für die Bestellung von Aufsatzkopien aus Zeitschriften. Prinzipiell gibt es zwei Verfahren, mit denen sich Bibliotheken an der automatisierten Fernleihe beteiligen können: das E-Mail-Verfahren und das SLNP-Verfahren. Auf beide wird im Handbuch eingegangen. Die automatisierte Fernleihe wurde im KOBV eingeführt, um die Fernleihe für die Benutzer zu beschleunigen, das Verfahren für die Bibliotheksmitarbeiter zu vereinfachen und den Arbeitsaufwand zu reduzieren. Sie basiert darauf, dass eine Bestellung anhand eines gefundenen Treffers ausgelöst wird – d.h. die bibliographischen Daten sind bereits verifiziert und in einem Katalog nachgewiesen. Anschließend wird die Bestellung über den ZFL-Server automatisch ausgeführt und verwaltet – sowohl in der regionalen KOBV-Fernleihe als auch in der verbundübergreifenden Fernleihe mit den deutschen Bibliotheksverbünden. Der ZFL-Server besteht aus verschiedenen technischen Komponenten. Eine dieser Komponenten ist das Bibliothekskonto, eine Internetanwendung, in der die Bestellverwaltung des ZFL-Servers für die Bibliotheksbediensteten transparent abläuft. Dazu hat jede Bibliothek im Bibliothekskonto eine eigene, Passwort-geschützte Dienstoberfläche. Im Laufe des Jahres 2009 hat die KOBV-Zentrale das Bibliothekskonto grundlegend überarbeitet; die neue Version wurde im September 2009 freigegeben. Neben der Überabeitung des Interfaces – so wird den Bibliotheken auf der Startseite nun eine Übersicht ihrer laufenden Bestellungen angezeigt und dient als direkter Einstieg in die Bearbeitung – wurde das Bibliothekskonto um folgende Funktionen erweitert: Bestellung zurücklegen (HOLD), Vormerkungen, Bestellungen zur Anfrage, Abbruch des Leitweges (auch verbundübergreifend), erweiterte Kommentarfunktion, Bestellnummernsuche in allen Verbünden. Das Handbuch, das die Vorgänge der Bestellverwaltung im Bibliothekskonto beschreibt, wurde in der nun vorliegenden 3. Auflage um die Beschreibung der neuen Funktionen ergänzt. An dieser Stelle ein Dank an die Kolleginnen und Kollegen aus den KOBV-Bibliotheken – Frau Bruske (UB der Freien Universität Berlin), Frau Ebert (UB der Europa-Universität Viadrina Frankfurt (Oder)), Frau Preuß (UB der Technischen Universität Berlin) und Herrn Ringmayer (Zentral- und Landesbibliothek Berlin) – für die tatkräftige Unterstützung bei der Entwicklung der neuen Funktionen.
    Keywords: ddc:020
    Language: German
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 5
    Publication Date: 2020-12-11
    Description: The Cooperative Library Network Berlin-Brandenburg (KOBV), Germany, addresses the problem of how to integrate resources found outside the library and library holdings into a single discovery tool. It presents a solution that uses open source technology to develop a next-generation catalog interface called the Library Search Engine. This pilot project was launched in 2007 with the library of Albert Einstein Science Park, Potsdam. The idea was to design and develop a fast and convenient search tool, integrating local holdings (books, journals, journal articles) as well as relevant scientific subject information such as open access publications and bibliographies.
    Keywords: ddc:020
    Language: English
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 6
    Publication Date: 2016-02-15
    Description: Wissenschaftliche Bibliotheken sind Vermittler von digitalen Medieninhalten. Sie müssen ihren Nutzern einen Zugang zu ihnen ermöglichen. Digitales Rechte Management (DRM), eingesetzt von den Verlagen, soll Nutzung und Zugang kontrollieren. Bibliotheken stehen DRM daher misstrauisch gegenüber, da dieses als Gefahr für die Wissenschaft und ihre (digitalen) Bibliotheken gesehen wird. Nur eine effektive Auseinandersetzung der wissenschaftlichen Bibliotheken mit der jeweiligen Politik der Verlage und den Verfahrensweisen bei DRM ermöglicht es ihnen, ihre Rolle als Vermittler und 'Gedächtnis der Menschheit' auch weiterhin erfolgreich wahrnehmen zu können. Unbestritten ist, dass DRM in seiner restriktiven Form die tägliche Arbeit der Bibliotheken erschwert. Deshalb müssen sie sich aktiv an der Standardisierung, der Entwicklung von Nutzungskonzepten und der Gestaltung der Rahmenbedingungen beteiligen.
    Description: Academic libraries are mediators of digital content. They have to ensure access for their patrons. Digital Rights Management (DRM), used by publishers, should control access and usage. Libraries mistrust DRM, because it is seen as a danger to scholarship, sciences and their (digital) libraries. Libraries only can persist as the 'archive of all human knowledge' if they start an effective controversy about the publishers' policies and if they know how DRM works. It is uncontentious that the restrictive form of DRM will complicate the everyday work of libraries. Therefore they have to engage in the prozess of standardization, in the development of concepts of usage and in the definition of general conditions of DRM.
    Keywords: ddc:020
    Language: German
    Type: masterthesis , doc-type:masterThesis
    Format: application/pdf
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  • 7
    Publication Date: 2020-12-11
    Description: Wissenschaftler sind an qualitativ hochwertiger Information interessiert, selten an Informationsversorgung selbst. Es ist ihnen in Fragen der Organisation meistens egal, von welchem Versorger sie das Material, das sie benötigen, bekommen. Sie wollen einfach nur alles, was sie brauchen, jederzeit, überall, sofort und möglichst kostengünstig oder gar kostenlos haben. Im Prinzip ist das möglich. Seit mindestens zehn Jahren werden so gut wie alle wissenschaftlichen Dokumente (Artikel, Messdaten,…) elektronisch erstellt. Eigentlich bräuchte man diese nur ins Internet zu stellen, und damit wäre alles verfügbar. Irgendwie funktioniert diese einfache Idee nicht so richtig, obwohl viele Anstrengungen von den verschiedensten Einrichtungen und Individuen unternommen werden, z. B. durch Open-Access-Bemühungen. Was sind die Gründe dafür? Die Fortschritte beim schnellen Zugriff auf Information im Internet sind atemberaubend (siehe Google), dennoch ist der zielgerichtete Zugriff auf wissenschaftlich relevante Information weiterhin nur oberflächlich vorhanden. Die Hindernisse sind vielfältiger Natur: Bequemlichkeit und Unwissen der Autoren, Gewohnheiten der Nutzer und Informationsvermittler, Barrieren durch Copyrights und Verlagsstrategien, Eitelkeiten. In diesem Artikel werden einige der Probleme erläutert, die dem Traum des Aufbaus der wissenschaftlichen Universalbibliothek entgegenstehen. Gleichzeitig wird skizziert, wie man auf dem Weg zur Verwirklichung des Traums ein Stück vorankommen und wie die zukünftige wissenschaftliche Informationsversorgung gestaltet werden kann.
    Keywords: ddc:020
    Language: German
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 8
    Publication Date: 2020-12-11
    Description: Bereits seit den siebziger Jahren katalogisieren Bibliotheken arbeitsteilig in Verbünden. Allerdings macht die Kooperation bislang oftmals an den Grenzen traditionell gewachsener Verbundstrukturen halt. Das ist ein Grund dafür, dass in Deutschland und Österreich das gleiche Buch im schlimmsten Fall an zahlreichen Stellen gleichzeitig katalogisiert wird, ohne dass der eine von der Arbeit des anderen profitiert. In dem folgenden Report werden erstmals konkrete Schritte beschrieben, die eine verteilte Katalogisierung über Verbundgrenzen hinweg verbessern. Dazu gehören Vereinbarungen für die Indexierung und die Suche über Z39.50, Regeln für gegenseitige Datenlieferungen und nicht zuletzt die Einführung einer eindeutigen Identifikationsnummer, die die erstkatalogisierende Institution vergibt. Der vorliegende Artikel ist ein vorläufiger Zwischenbericht der von der Arbeitsgemeinschaft der Verbundsysteme eingesetzten Arbeitsgruppe „Kooperative Neukatalogisierung“.
    Keywords: ddc:020
    Language: German
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 9
    Publication Date: 2024-01-12
    Description: Im Kooperativen Bibliotheksverbund Berlin-Brandenburg (KOBV) wird für die Online-Fernleihe der Zentrale-Fernleihserver (ZFL-Server) der Firma Sisis eingesetzt. Die Software ist in der KOBV-Zentrale installiert. Der ZFL-Server dient im KOBV sowohl für die Bestellung von Monographien als auch für die Bestellung von Aufsatzkopien aus Zeitschriften. Prinzipiell gibt es zwei Verfahren, mit denen sich Bibliotheken an der Online-Fernleihe beteiligen können: das E-Mail-Verfahren und das SLNP-Verfahren. Auf beide wird im Handbuch eingegangen. Die Online-Fernleihe wurde im KOBV eingeführt, um die Fernleihe für die Benutzer zu beschleunigen, das Verfahren für die Bibliotheksmitarbeiter zu vereinfachen und den Arbeitsaufwand zu reduzieren. Sie basiert darauf, dass eine Bestellung anhand eines gefundenen Treffers ausgelöst wird – d.h. die bibliographischen Daten sind bereits verifiziert und in einem Katalog nachgewiesen. Anschließend werden die Fernleihbestellungen über den ZFL-Server automatisch ausgeführt und verwaltet – sowohl in der regionalen KOBV-Fernleihe als auch in der verbundübergreifenden Fernleihe mit den deutschen Bibliotheksverbünden. Der ZFL-Server besteht aus verschiedenen technischen Komponenten. Eine dieser Komponenten ist das Bibliothekskonto, eine Internetanwendung, in der die Bestellverwaltung des ZFL-Servers für die Bibliotheksbediensteten transparent gemacht wird. Sowohl für die aktive als auch für die passive Fernleihe ist im Bibliothekskonto der Status der Bearbeitung zu jedem Zeitpunkt ersichtlich, z.B. in welcher Bibliothek sich die Bestellung gerade befindet, wann sie dort eingegangen ist und wann sie weggeschickt wurde, ob mit positivem oder negativem Ergebnis. Das Bibliothekskonto ist damit für die Bibliothek ein komfortables Instrument zum Überwachen der Fernleihbestellungen, in dem sie zudem – falls notwendig – in den Bestellvorgang eingreifen kann. Dazu hat jede Bibliothek im Bibliothekskonto eine eigene, Passwort-geschützte Dienstoberfläche. Das vorliegende Handbuch beschreibt die Vorgänge der Bestellverwaltung im Bibliothekskonto. Es richtet sich an Bibliotheksmitarbeiter, die sich mit den einzelnen Arbeitsschritten der Online-Fernleihe vertraut machen wollen. Darüber hinaus ist es zum Nachschlagen gedacht, wenn sich in der täglichen Arbeit Unklarheiten ergeben.
    Keywords: ddc:020
    Language: German
    Type: reportzib , doc-type:preprint
    Format: application/pdf
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  • 10
    Unknown
    Hershey, PA : Idea Group Pub
    Keywords: Electronic books ; Internet marketing
    Pages: 1 v. (various pagings)
    ISBN: 1-591-40826-1
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  • 11
    Keywords: Electronic books ; Electronic commerce, Management ; Information technology, Management ; Technological innovations, Management
    Pages: 1 v. (various pagings)
    ISBN: 1-591-40631-5
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  • 12
    Unknown
    Cheltenham, UK ; Northampton, MA : Edward Elgar
    Keywords: Electronic books ; Environmental policy, Australia ; Industries, Case studies, Environmental aspects, Australia
    Pages: ix, 216 p.
    ISBN: 1-8454-2572-3
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  • 13
    Unknown
    Cheltenham, U.K ; Northampton, Mass : Edward Elgar
    New horizons in international business  
    Keywords: Corporate governance ; Corporations, Growth ; Electronic books ; International business enterprises, Management ; International economic relations ; Investments, Foreign, Government policy
    Pages: 1 v. (various pagings)
    ISBN: 1-8454-2557-X
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  • 14
    Unknown
    London ; Sterling, Va : Millward Brown/Kogan Page
    Keywords: Advertising, Psychological aspects ; Advertising, Research ; Electronic books ; Human information processing, Research
    Pages: xxiv, 232 p.
    ISBN: 1-423-71114-9
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  • 15
    Unknown
    London ; Sterling, VA : Kogan Page
    Keywords: Business enterprises, Environmental aspects ; Business ethics ; Electronic books ; Factory and trade waste, Environmental aspects ; Industrial management ; Pollution prevention ; Small business, Environmental aspects ; Social responsibility of business
    Pages: xv, 485 p.
    ISBN: 1-423-70883-0
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  • 16
    Unknown
    Cambridge, U.K ; New York, N.Y : Cambridge University Press
    Keywords: Cellular telephone services industry ; Electronic books ; Mobile communication systems, Economic aspects ; Wireless communication systems, Economic aspects
    Pages: 1 v. (various pagings)
    ISBN: 0-511-11564-4
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  • 17
    Unknown
    Cambridge ; New York : Cambridge University Press
    Keywords: Shakespeare, William, Tragedies ; Electronic books ; Identity (Psychology) in literature ; Tragedy ; Violence in literature
    Pages: ix, 228 p.
    ISBN: 0-511-11352-8
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  • 18
    Keywords: Electronic books ; Finance ; Finance, History
    Pages: viii, 195 p.
    ISBN: 1-8454-2573-1
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  • 19
    Unknown
    New York : Cambridge University Press
    Keywords: Capital market ; Electronic books ; Futures market ; Stock exchanges
    Pages: 1 v. (various pagings)
    ISBN: 0-511-11580-6
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  • 20
    Unknown
    Abingdon : Helicon Pub
    Keywords: Art, Dictionaries ; Electronic books ; Signs and symbols, Dictionaries
    ISBN: 1-423-71132-7
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  • 21
    Keywords: Business enterprises, Computer networks ; Electronic books
    Notes: Who do you know? -- The seven keys to a powerful network -- Face-to-face vs. virtual communications -- Introduction to social software -- Email lists -- Relating in real-time -- Virtual communities -- Web logs (blogs) -- Social visibility software -- Virtual becoming reality -- The future of social software -- Netiquette -- Manage the email deluge -- The virtual you -- Privacy, safety, and other concerns -- Increase your character -- Increase your competence -- Build the relevance level of your network -- Build strong ties -- Increase the level and quality of information -- Grow the number of people in your network -- Increase the diversity of your network -- Ten simple steps to radically improve your network online -- Finding a job -- Marketing -- Sales -- Business development -- Volunteering
    Pages: 1 v. (various pagings)
    ISBN: 0-8144-2893-2
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  • 22
    Unknown
    Cambridge ; New York : Cambridge University Press
    Keywords: Shakespeare, William, Language ; Shakespeare, William, Romeo and Juliet ; Shakespeare, William, Stage history, 1950- ; Shakespeare, William, Stage history, England, London ; Electronic books ; English language, Pronunciation, Early modern, 1500-1700 ; Globe Theatre (London, England : 1996- )
    Pages: xviii, 188 p.
    ISBN: 0-511-11364-1
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  • 23
    Unknown
    Cambridge, U.K ; New York : Cambridge University Press
    Keywords: Electronic books ; Religion, Study and teaching (Higher) ; Theology, Study and teaching (Higher)
    Pages: xvii, 230 p.
    ISBN: 0-511-11355-2
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  • 24
    Unknown
    Northhampton, Mass : Edward Elgar Pub
    New horizons in international business  
    Keywords: Japan, Economic conditions, 1945- ; Japan, Economic policy, 1945- ; Electronic books ; Industries, Japan
    Pages: 1 v. (various pagings)
    ISBN: 1-8454-2567-7
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  • 25
    Keywords: Electronic books ; Motion pictures, Dictionaries
    ISBN: 1-423-71126-2
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  • 26
    Unknown
    Ottawa : International Development Research Centre
    Keywords: Electronic books ; Electronic commerce, Case studies, Asia
    Notes: Action research on e-commerce for small artisans and development organizations : Pan-Asia E-commerce / Aniceto C. Orbeta, Jr -- Direct marketing of artisanal products through the Internet / Rajveer Singh -- E-marketers : an innovative approach to e-commerce / Loyola Joseph and Santosh Narayanan -- Impact of policy on development of e-commerce in Vietnam / Tran Ngoc Ca
    Pages: xi, 99 p.
    ISBN: 1-552-50179-5
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  • 27
    Unknown
    Cheltenham, U.K ; Northampton, Mass : Edward Elgar
    Keywords: European Union countries, Appropriations and expenditures ; Electronic books ; Finance, Public, Auditing, European Union countries ; Fiscal policy, European Union countries
    Pages: xvi, 256 p.
    ISBN: 1-8454-2560-X
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  • 28
    Unknown
    Cambridge, UK ; New York : Cambridge University Press
    Keywords: Autonomy (Psychology) ; Electronic books ; Ethics, Modern
    Notes: Planning agency, autonomous agency / Michael E. Bratman -- Autonomy without free will / Bernard Berofsky -- Autonomy and the paradox of self-creation : infinite regresses, finite selves, and the limits of authenticity / Robert Noggle -- Agnostic autonomism revisited / Alfred R. Mele -- Feminist intuitions and the normative substance of autonomy / Paul Benson -- Autonomy and personal integration / Laura Waddell Ekstrom -- Responsibility, applied ethics, and complex autonomy theories / Nomy Arpaly -- Autonomy and free agency / Marina A.L. Oshana -- The relationship between autonomous and morally responsible agency / Michael McKenna -- Alternative possibilities, personal autonomy, and moral responsibility / Ishtiyaque Haji -- Freedom within reason / Susan Wolf -- Procedural autonomy and liberal legitimacy / John Christman -- The concept of autonomy in bioethics : an unwarranted fall from grace / Thomas May -- Who deserves autonomy, and whose autonomy deserves respect? / Tom L. Beauchamp -- Autonomy, diminished life, and the threshold for use / R.G. Frey
    Pages: ix, 350 p.
    ISBN: 0-511-08224-X
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  • 29
    Unknown
    Palo Alto, CA : Stanford University Press
    Latin American development forum series  
    Keywords: Latin America, Economic conditions ; Economic stabilization, Latin America ; Electronic books ; Macroeconomics ; Structural adjustment (Economic policy), Latin America
    ISBN: 0-8213-5820-0
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  • 30
    Unknown
    Cheltenham, U.K ; Northampton, Mass : Edward Elgar
    Keywords: Economic assistance, Developing countries ; Economic development ; Electronic books ; Public administration, Developing countries
    Pages: x, 190 p.
    ISBN: 1-8454-2552-9
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  • 31
    Keywords: Wolfensohn, James D. ; Economic development, Finance ; Electronic books ; World Bank
    Pages: viii, 156 p.
    ISBN: 0-8213-6174-0
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  • 32
    Keywords: Electronic books ; World Bank
    Pages: xix, 546 p.
    ISBN: 0-8213-6157-0
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  • 33
    Unknown
    Kalamazoo, Mich : W.E. Upjohn Institute for Employment Research
    Keywords: Electronic books ; Insurance, Unemployment ; Insurance, Unemployment, Cross-cultural studies
    Notes: Economic performance and unemployment -- Unemployment protection -- Unemployment compensation in the OECD-20 countries -- Unemployment compensation in the CEE-FSU countries -- Unemployment compensation in East and South Asia -- Unemployment compensation in Latin America and Caribbean countries -- Three problem areas for unemployment compensation programs -- Concluding remarks
    Pages: 1 v. (various pagings)
    ISBN: 1-417-59635-X
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  • 34
    Unknown
    London ; Philadelphia : Jessica Kingsley Publishers
    Keywords: Child welfare, Research, Great Britain ; Children of minorities, Services for, Great Britain ; Electronic books ; Family social work, Great Britain ; Social work with minorities, Great Britain
    Pages: 255 p.
    ISBN: 1-423-71058-4
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  • 35
    Unknown
    Cheltenham, U.K ; Northampton, Mass : Edward Elgar Pub
    Keywords: Electronic books ; Employee motivation, Europe ; Hours of labor, Flexible, Europe ; Incentives in industry, Europe ; Insurance, Unemployment, Europe ; Labor market, Europe ; Labor supply, Europe
    Pages: 1 v. (various pagings)
    ISBN: 1-8454-2562-6
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  • 36
    Unknown
    Cheltenham, U.K ; Northampton, Mass : Edward Elgar
    Keywords: Electronic books ; Euro area, Congresses ; Euro, Congresses ; International finance, Congresses ; Monetary policy, Congresses
    Pages: viii, 163 p.
    ISBN: 1-8454-2566-9
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  • 37
    Keywords: Business planning ; Conglomerate corporations, Management ; Conglomerate corporations, Planning ; Corporate culture ; Corporations, Growth ; Electronic books
    Notes: The challenge of new businesses -- Beating the odds -- The difficulties of building new legs -- When low growth is better than gambling -- The new business traffic lights -- Diversification -- Searching for new businesses -- Is there a role for corporate venturing? -- Positioning and supporting a new business -- An age of realism
    Pages: xv, 321 p.
    ISBN: 1-417-59769-0
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  • 38
    Unknown
    New York, NY : Springer Science+Business Media
    Monographs in computer science  
    Keywords: Electronic books ; Object-oriented programming (Computer science) ; Reverse engineering
    Pages: xiv, 208 p.
    ISBN: 0-387-23803-4
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  • 39
    Unknown
    Washington, D.C : World Bank
    Keywords: Bankruptcy, Congresses ; Consolidation and merger of corporations, Congresses ; Corporate reorganizations, Congresses ; Electronic books ; Financial crises, Congresses ; International finance, Congresses
    Pages: xlix, 382 p.
    ISBN: 0-8213-6225-9
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  • 40
    Unknown
    North Hampton, Mass : Edward Elgar
    Keywords: Capitalism, Moral and ethical aspects ; Democracy, Moral and ethical aspects ; Economics, Moral and ethical aspects ; Electronic books ; Social justice ; Social responsibility of business ; Social security, Moral and ethical aspects ; Welfare state, Moral and ethical aspects
    Pages: 1 v. (various pagings)
    ISBN: 1-8454-2570-7
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  • 41
    Unknown
    Northampton, Mass : Edward Elgar Pub
    Keywords: Electronic books ; Environmental economics ; Environmental policy ; Institutional economics
    Pages: 1 v. (various pagings)
    ISBN: 1-8454-2574-X
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  • 42
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 2 (1964), S. 1-8 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The results of electrophoresis experiments on aqueous solutions of native and thermally denatured DNA are reported. A significant decrease of the electrophoretic mobility has been observed following thermal denaturation, which under suitable conditions gives rise to a resolution into two peaks of 1 : 1 mixtures in the electrophoretic pattern. This result is entirely consistent with the previously reported increase of the activity coefficient of sodium counterions following thermal denaturation. The hypothesis that thermal denaturation of calf thymus DNA induces a large decrease of charge density on the macroion which has been ascribed to the population of more extended conformations of the chains in the disordered region of the molecule is therefore further confirmed.
    Additional Material: 4 Ill.
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  • 43
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the depolymerization of native dextran in dilute hydrochloric acid at different temperatures has been followed by measurements of M̄w, M̄n, [η], 〈ρ2〉1/2, and S. The data allow the correlation of the various parameters of the total hydrolyzate at various degrees of depolymerization. At a first approximation the results conform to a random splitting of a statistical, branched polymer.
    Additional Material: 5 Ill.
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  • 44
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The γ-ethyl-L-glutamate NCA polymerization initiated by di-n-butyl and di-isopropyl amine was studied. The experimental kinetic curves show an autocatalytic portion with 25-30% conversion, followed by a pseudo first-order region which extends up to at least 85-90%. In this linear region, the reaction order appears to be 0.5 in initiator with both amines. High degrees of polymerization and high reaction rates were observed. These results are similar to those obtained in the γ-benzyl-L-glutamate NCA polymerization initiated by sodium methoxide.
    Additional Material: 5 Ill.
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  • 45
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dielectric constant and the electric birefringence of poly-γ-benzyl-L-glutamate in ethylene dichloride-dichloroacetic acid mixtures have been measured as functions of the solvent composition. These properties undergo a marked decrease with the addition of a small amount of dichloroacetic acid, as well as an abrupt change accompanying the helix-coil transition in the vicinity of 75 vol.-% dichloroacetic acid. The former is attributed to the apparent diminution of the dipole moment of helical poly-γ-benzyl-L-glutamate molecule, which may be due to the protonation of terminal amide groups.
    Additional Material: 7 Ill.
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  • 46
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 2 (1964) 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 47
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of γ-benzyl-L-glutamate NCA initiated by n-hexylamine in DMF proceeds with two successive propagation rates whose ratio is about 1.5. The onset of the increase in rate of propagation occurred at a DPn of 7-14, which was independent of initiator to anhydride ratio and anhydride concentration and not a result of anhydride impurities. The increase in rate is likely a result of a conformational change in the polymer at a DPn of 7-14.
    Additional Material: 1 Ill.
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  • 48
    Electronic Resource
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    New York : Wiley-Blackwell
    Biopolymers 2 (1964), S. 147-161 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The NCAs of the N-benzyl derivatives of β-alanine, β-DL-aminobutyric acid, and β-DL-aminoisobutyric acid (nonplanar six-membered rings) were prepared by reacting the corresponding N-chloroformyl derivatives, obtained on reaction of the N-benzyl amino acids with phosgene, with triethylamine. Contrary to the others, the NCA of N-benzyl-β-alanine polymerized readily on heating in vacuo or in solution, using n-hexylamine or methanolic sodium methoxide as initiators. With n-hexylamine the molecular weights of the polymers obtained in benzene, dioxan, and dimethylsulfoxide, were in accordance with DP = [NCA]/[Initiator], as was found with conventional five-membered ring NCAs of α-amino acids. With sodium methoxide initiation, DPs of the polymers obtained were smaller than the (NCA)/[Initiator] ratio, contrary to what was found previously with α-amino acid NCAs. The possibility that stereochemical factors are responsible for the differences in polymerization activity of various. N-alkyl β as well as α amino acid NCAs is discussed.
    Additional Material: 4 Ill.
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  • 49
  • 50
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    Biopolymers 2 (1964), S. 231-236 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electrophoretic mobility of DNA in the presence of tetramethylammonium and alkali metal ion chlorides has been studied as a function of ionic strength. Each cation exhibits a characteristic behavior in accord with the idea that the order of inter-action with DNA is Li+ 〉 Na+ 〉 K+ 〉 TMA+. The application of theories of the electrophoresis of polyelectrolytes is discussed, leading to an attempt to calculate the fractional charge per DNA phosphorus from the mobility data. Over the range 0.05-0.4M a constant and unique value of the DNA charge is obtained in the presence of each cation. Values of the zeta potential and of the friction factor per monomer unit are also calculated.
    Additional Material: 1 Ill.
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  • 51
    Electronic Resource
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    Biopolymers 2 (1964), S. 135-146 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple quantitative theory of inactivation of transforming DNA has been formulated. It is based on the idea that genetic recombination of the molecule of transforming DNA with the bacterial genome is possible only, from the point mutation of the gene up to the nearest hit or point of damage on the corresponding DNA molecule. Our data and the data of other authors on the kinetics of inactivation by HNO2 or U.V. light or both are consistent with these theoretical predictions. Theoretical predictions were made concerning the extent of reactivation by fusion mid annealing of damaged DNA with a diluting genetically inactive DNA. These estimates have been reasonably confirmed by our experimental results.
    Additional Material: 7 Ill.
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  • 52
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    Biopolymers 2 (1964), S. 15-25 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In order to study the effect of glucose substitution on the sedimentation velocities of the T-even phage DNA's, T2 and T2*, and T6 and T6* bacteriophages were grown with H3and P32 labeling. Zone sedimentation of the DNA's isolated from these phagea showed that the glucosylated DNA's from both T2 and T6 sediment faster than the nonglucosylated molecules. Nonglucosylated DNA from TG and T2 phages sedimented with the same velocity, suggesting that the molecules of these phages are of the same length.
    Additional Material: 6 Ill.
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  • 53
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    Biopolymers 2 (1964), S. 43-49 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We report a simple method for measuring partial specific volumes, of polymers in dilute solutions with an accuracy of 3 parts per thousand. This method has been applied to 7 polypeptides in 4 organic solvents. The residue volumes deduced from these data are compared to those calculated by a differential method. The discrepancy is generally of the order of 1.5%.
    Additional Material: 3 Tab.
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  • 54
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    Biopolymers 2 (1964), S. 283-286 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 55
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 2 (1964) 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 56
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: It is shown that the formation of the three-strand poly (A + 2U) complex is accompanied by a decrease in optical absorbance at 280 mμ, while the format ion of poly (A + U) is not. This difference makes it possible to demonstrate that in dilute solutions (∼10-4 monomolar), a 1 : 1 mixture of poly A and poly U always forms poly (A + U) at room temperature. At higher temperatures in solutions containing more than about 0.2M sodium ion, poly (A + U) is converted to poly (A + 2U) and free poly A. These results are consistent with the observations reported by Miles and Frazier, using infrared absorption spectra, at much higher polymer concentrations. It is concluded that most of the physicochemical studies of 1 : 1 mixtures of poly A and poly U in dilute aqueous solution refer to the two-stranded species.A simple thermodynamic analysis is developed to explain the two- to three-strand conversion, and with the use of a “phase diagram” showing conditions of stability of the various poly A-poly U structures as a function of salt and temperature, it is possible to estimate the value of the enthalpy of formation of poly (A + 2U).
    Additional Material: 8 Ill.
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  • 57
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    Biopolymers 2 (1964), S. 337-347 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using a chromatographic technique, the adsorption of the polyribonucleotides s-RNA and poly-A provided with tri-n-butylammonium ions from an aqueous solution on to the surface of polymeric hydrocarbon granules has been demonstrated. The aqueous solution from which adsorption takes place is the aqueous phase which results on agitating together n-butanol (100), water (130), tri-n-butylamine (10), n-butyl ether (10), and glacial acetic acid (2.5) (parts by volume). Microporous polyethylene granules, microporous fluorinated polyethylene granules, and solid grains of polyethylene powder have been employed as adsorbents. The adsorbed polyribonucleotides could be eluted by aqueous solutions of sodium chloride, urea, or triethylammonium acetate. s-RXA with tri-n-butylammonium counterions could also be adsorbed on polymethacrylic acid in tri-n-butylammonium form and eluted therefrom with aqueous urea solutions. It is considered that the adsorption from aqueous solution of polyribonucleotides with tri-n-butylammonium counterions on polymeric hydrocarbon surfaces is mediated by hydrophobic bond formation. Van der Waals forces may also contribute to the bonding. It is suggested that studies on the adsorption of polynucleotides provided with counterions: possessing nonpolar groups at an aqueous solution-polymeric hydrocarbon interlace may permit the elaboration of experimental systems to serve as models for the evaluation of the role of hydrophobic and van der Waals bonding forces in the interaction of polynucleotides with cell membrane surfaces.
    Additional Material: 5 Ill.
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  • 58
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    Biopolymers 2 (1964), S. 395-398 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 59
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    Biopolymers 2 (1964), S. 361-380 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Deoxyribonucleic acids (DNA's) extracted from several biological sources have been studied by means of the flow dichroism method, using the transparent coaxial cylinder apparatus. This study has two purposes: (1) to make clear the hydrodynamic behavior of the DNA chain, and the regularity in the orientation of purine and phrimidine bases about the molecular axis; and (2) to develop this particular flow dichroism method as an established device for the study of chain regularity of DNA and other chain polymers. The velocity gradient dependence of dichroism agrees well, to a first approximation, with the behavior of a model of a hydrodynamically equivalent ellipsoid in revolution. Differences between theoretical and empirical curves have been tentatively ascribed to the flexibility of the chain under consideration. Two kinds of data, 1 lie rotary diffusion coefficient and internal dichroism, have been evaluated by a graphical device in which the double logarithmic plots of reduced dichroism and velocity gradient of flow are compared with the theoretical curve. The data obtained have shown good reproducibility for DNA samples prepared by the same method from the same biological source. However, a remarkable difference in internal dichroism and rotary diffusion constant has been observed between DNA groups of different biological origin. The difference may be caused by fragmentation of DNA during the deproteinization procedure, bill the possibility that some of these differences originate in the biological source of the DNA cannot be denied. Orientation of purine and phrimidine bases in aqueous solution is found to be quite regular in direction, as predicted by the Watson-Crick model. Dichroic spectra have shown that the direction of the oscillator dipole corresponding to the 260 mμ absorption band has a different angular relationship to the helical axis than the oscillator dipole for the 220 mμ band.
    Additional Material: 11 Ill.
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  • 60
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    Biopolymers 2 (1964), S. 381-393 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A study of the super helical structure of synthetic polypeptides, such as poly-γ-benzyl-D (or L)-glutamate (PBDG or PBLG) was carried out. The PEG was dissolved in dimethylformamide (DMF). The solution was either allowed to remain at room temperature for a long time or poured into some fatty acid, such as formic acid, acetic acid, propionic acid, or caprylic acid. Whether the polymer precipitated slowly or rapidly depended upon the aging of the solution or the nature of the acid used. The precipitated gels revealed the coiled coil fibrils, but the feature and degree of coiling varied, depending upon the length of aging or the nature of the acid used for precipitation. After a short aging of the solution, there was no helical structure in the gels. After long aging, very fine-coiled coil macrofibrils or small spindle-like fibrils were obtained. The macrofibrils consisted of the spindle-like fibrils which in turn consisted of microfibrils (diam. 60-70A.). When using the fatty acid precipitation very fine to medium fine super helices were obtained. Extremely fine super helices were obtained in propionic acid. In these gels the PBG chains have an α-helical conformation. When PMLG-DCA solution was stored for a long time, another type of precipitation was obtained, one giving evidence of so-called cross-β crystallization and no coiled coil fibrils. The precipitation of cross-β fibrils was obtained when the concentration of the solution was above 8%.
    Additional Material: 12 Ill.
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  • 61
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    Biopolymers 2 (1964) 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 62
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    Biopolymers 2 (1964), S. 399-413 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Titration studies of the 1 : 1 helical polynucleotide complex of polyinosinic acid and polycytidylic acid reveal that these two polymers form a complex when the polycytidylic acid is protonated near pH 3. Sedimentation studies show that the protonated complex also has a 1 : 1 stoichiometry. However, the protonated complex is more stable than the unprotonated neutral complex as judged by its thermal stability. The molecular structure of the protonated complex is not the same as the neutral form. Study of the kinetics of the reaction of the protonated complex with formaldehyde suggests that the amino group of cytosine is involved in hydrogen bonds which hold the polynucleotide strands together.
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  • 63
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    Biopolymers 2 (1964), S. 415-444 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The protein sequences now known have been reconstructed as a kind of intriguing logical-mathematical puzzle using information about fragments of the molecules. We wish to show that the reconstruction can be done systematically by repeating a series of elementary operations on these same data governed by a set of well-defined rules. The completely automatic reconstruction of polymer sequences by a high speed digital computer using these operations and rules is demonstrated.
    Additional Material: 1 Ill.
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  • 64
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mechanism of the renaturation of DNA molecules is examined on the basis of the bimolecular interaction of Gaussian chain polymers. In the nucleus formation by hydrogen bonding in segment-segment interaction, two types of interchain interaction, that is, one between complementary chains and one between noncomplementary chains, and one noncomplementary intrachain interaction are considered to be, in competition. Several previously observed characteristics of the renaturation process are displayed by this simple model. In particular it accounts for the dependence of the extent of renaturation on the heterogeneity, molecular weight, and radius of gyration of DNA, and of the ratios of the reaction rates between complementary and noncomplementary segments. Among these variables the ratio of reaction rates has shown to have a quite specific value, as high as the order of 104, which favors the complementary-strand interaction. This very great bias in favor of complementary strand interaction emphasizes that the renaturation phenomena displays the same character of biological specificity that is associated with enzyme-substrate interaction or antigen-antibody interaction. Moreover, since DNA is a good example of a one-dimensional system, it seems to provide a suitable clue for pursuing the analysis of pattern recognition at the macromolecular level.
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  • 65
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    Biopolymers 2 (1964), S. 463-481 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The polymerization of DL-β-Phenylalanine N-carboxy anhydride adsorbed on polysarcosine dimethylamide has been studied further. This unusual reaction, which is analogous kinetically to reactions catalyzed by enzymes, was called the “chain-effect.” For polymerization of N-carboxy anhydrides by this mechanism it is necessary that the initiating polymer should possess an adsorption site and a terminal base group. The effect is shown to occur with simple compounds such as amino acid dimethylamides but not with poly-L-proline due to the inability of this polymer to adsorb the anhydride. From a study of the reaction of block copolymers of L-proline and sarcosine with DL-β-phenylalanine it is concluded that the relative positions of the adsorption site and terminal base group do not greatly influence the reaction rate, but the accessibility of the adsorption sites is an important factor determining the reactivity of polysarcosine dimethylamides of various degrees of polymerization (n). At high values of n the polymer exists in a coiled form and only those sites close to the terminal base group participate in the reaction. Initial rate studies give a detailed description of the early stage of the chain-effect polymerization. With these data and by use of analog computer techniques the complete reaction has been studied. It is concluded that the poly-DL-β-phenylalanine block produced is not permanently attached to the polysarcosine chain by hydrogen bonds during its formation but that an equilibrium exists between the polysarcosine and the poly-DL-phenylalanine blocks.
    Additional Material: 6 Ill.
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  • 66
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Del Re's method for the study of saturated compounds has been adapted so as to deal with the σ-framework of conjugated molecules. This modified procedure is used in evaluating the σ-contribution to the dipole moments of the nucleic bases and of the A-T and G-C base pairs and also to the free energy change in the tautomeric, equilibria of the bases. Associated with an appropriate Hückel method for evaluating the π-contribution, the results obtained predict a small resultant moment for A-T versus a large moment for G-C. The energy calculations predict the keto and amino forms of the bases to be the most stable forms and cytosine to be the most easily involved in tautomeric shift to the rare form.
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  • 67
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    Biopolymers 2 (1964) 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 68
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Temperature jump measurements employing optical rotation to follow transients show an upper limit of 10μsec. on the half time of the helix-random coil relaxation in poly-α, L-glutamic acid. No relaxations are observed under conditions where the polymer exists in completely helical or completely random coil form. Assuming that the helix-coil transition can be described kinetically as a pure growth process, expressions for the relaxation time are derived for three special cases. A comparison is made between the rate of the helix-coil transition and the rate of imide proton exchange.
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  • 69
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    Biopolymers 2 (1964), S. 501-501 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 70
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    Biopolymers 2 (1964), S. 561-574 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Numerical calculations have been done on the exciton spectrum of a schematic model of a linear polymer. The model consists of a random sequence of two kinds of subunit whose energy levels and transition moments are almost, but not quite, the same. The orders of magnitude of parameters are taken from DNA, but the full helical geometry has not been considered. Results are given for the density of energy levels, the dipole transition strength per unit energy, and the distribution of excitation energy along the polymer in individual states. A number of localized exciton states were found.
    Additional Material: 6 Ill.
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  • 71
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    Biopolymers 2 (1964) 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 72
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    Biopolymers 2 (1964), S. 9-14 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A calculation based upon Gorin's equation for the electrophoresis of a rigid cylinder is used to compare the available results of electrophoresis and membrane equilibrium experiments on DNA. The distribution of chloride ions across a membrane impermeable to DXA is considered. For a reasonable choice of parameters, agreement within about 2% is obtained between the values calculated from electrophoresis and the results of membrane equilibrium studies over a twenty-fold range of NaCl concentration.
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  • 73
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Light-scattering, sedimentation, viscosity, and reducing power measurements have been carried out on a sample of native dextran from Leuconostoc mesenteriodes B-512. The results are discussed in relation to the structure, polydispersity, and branching of the polysaccharide. The effect of different solvents on the behavior of native dextran has been studied. The molecular weight of the dextran remains unchanged in all the solvents used, while the radius of gyration shows a significant increase in some of them (concentrated salts, urea, and glucose solutions); in water-methanol solutions the radius of gyration slightly decreases.
    Additional Material: 3 Ill.
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  • 74
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    Biopolymers 2 (1964), S. 65-68 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The statistical mechanical theory of the helix-coil transition of DNA has been recently discussed by one of the authors, who considered an assembly of DNA molecules with a Markoff distribution of nucleotide sequences. The present communication improves upon the above mentioned theory by introducing approximate normalization factors for the unnormalized statistical weights of finding a given molecule of the assembly in a given microscopic state.
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  • 75
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    New York : Wiley-Blackwell
    Biopolymers 2 (1964), S. 103-103 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 76
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    New York : Wiley-Blackwell
    Biopolymers 2 (1964), S. 79-89 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of small quantities of metal ions on the electrophoretic mobility of calf thymus DNA in solutions maintained at 0.2 ionic strength with weakly interacting (CH3)4N+ ions yields information about interactions occurring in a region very close to the polymer chain. By means of this technique, it is demonstrated that the binding order to DNA is Li+ 〉 Na+ 〉 K+ for the alkali metal ions and Mn++ 〉 Mg ++ 〉 Ca++ for the divalent ions studied. The quantitative details are compared to earlier work on the long-chain polyphosphates. Close agreement between the two systems is obtained indicating that an intrinsic property of individual phosphate groups is being observed and that minor discrepancies probably arise from secondary factors. Three types of stability constants representing the binding of alkali metal ions to DNA are calculated and although differing in absolute magnitude, they all satisfactorily represent the result that the order of interaction is Li+ 〉 Na+ 〉 K+ with respective relative strengths of 1.5 : 1 : 0.8.
    Additional Material: 2 Ill.
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  • 77
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    Biopolymers 2 (1964), S. 113-121 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Birefringence relaxation times on removing the electric field characterize the rigidity of a flexible linear macromolecule structure. Electrical birefringence investigation of DNA solutions supports this view. This principal regularities displayed by relaxation times of electric birefringence decay curves in solutions of chain macromolecules are considered.
    Additional Material: 6 Ill.
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  • 78
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 186-189 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: m-Dinitro-benzol und einige seiner Derivate (I, II, VII) lassen sich durch aufein-anderfolgende Einwirkung von Alkylmagnesiumhalogeniden, Methylamin/Formaldehyd und Essigsäure zu Mannich-Verbindungen von Dinitrodialkylcyclohexenen (Vb-e, VIII) umsetzen.
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  • 79
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 132-139 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 3-Brom-cyclo-penten,-hexen und-hepten reagieren mit Lithiumaluminiumhydrid unter Bildung der jeweiligen cyclischen Monoolefine. Ann substituierten 3-Brom-cyclohexenen wurde gezeigt, daß die Reaktion sowohl als einfache nucleophile Substitution des Broms durch Wasserstoff als auch unter Allylumlagerung mit Angriff des Hydridions am C-Atom 1 verläuft. Die in beiden Allylstellungen bromierten cyclischen Olefine reagieren mit Lithiumaluminiumhydrid unter Bildung mehrerer Produkte, die durch Angriff des Hydrids an einem halogentragenden C-Atom (a), an einem olefinischen C-Atom (b) und an einem Brom-atom (c) entstanden sind. Reaktion (a) liefert Monoolefin, (b) ergibt 4-Bromolefin und nach (c) entsteht 1.3-Diolefin. Die Eliminierung nach (c) wurde allerdings nur am unsubstituierten Cyclohexen- und Cycloheptendibromid beobachtet. Für die Eliminierung wird ein weitgehend koplanarer Übergangszustand angenommen, der bei den anderen untersuchten Dibromiden nicht möglich ist.
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  • 80
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 165-168 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Desaminierung des 9-Amino-Δ4(10)-octalins in essigsaurer Lösung gibt zu etwa 80% die substituierten Allylalkohole Δ9(10)-Octalol-(1) und Δ4(10)-Octalol-(9) nebst Acetat, sowie die aus diesen durch normale Wasserabspaltung hervorgehenden Hexaline.
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  • 81
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 179-185 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei der Umsetzung von β-Phenäthylmercaptan mit Aldehyden und Chlorwasserstoff entstehen [α-Chlor-alkyl]- β-phenäthyl-sulfide, die mit Aluminium-chlorid unter Ringschluß zu Isothiochromanen reagieren. - 1-Chlor-isothio-chroman, durch Einwirkung von Chlor auf Isothiochroman gewonnen, liefert mit Alkyl- oder Arylmagnesiumhalogeniden 1-Alkyl- bzw. 1-Aryl-isothiochromane, mit Mercaptanen 1-Alkylmercapto-, mit sekundären Aminen 1-Di-alkylamino- und mit Alkoholen 1-Alkoxy-isothiochromane. - Durch Umsetzung der letzteren mit Natriumhydrogensulfit entsteht Isothiochroman-sulfonsäure-(1), die in Isothiochroman-S-dioxid-sulfonsäure-(1) bzw. deren Ester übergeführt werden kann.
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  • 82
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 218-224 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1.2-Benzpyren gibt der Bromierung das 5.8-Dibromderivat II und bei der Chlorierung das 3.5.8.10-Tetrachlorderivat V. Aus II wird das 5.8-Dinitril III und daraus die entsprechende Dicarbonsäure IV dargestellt. Die Hydrierung des 1.2-Benzpyrens führt zunächst zu einer Hexahydroverbindung, die ein Anthracenderivat ist, und dann zu dem Decahydro-1.2-benzpyren VI, das einen Naphthalinkern enthält. Die Oxydation verläft sehr komplex und liefert neben dunklen Kondensationsprodukten nur geringe Mengen zweier Säuren, die bei der Decarboxylierung Phenanthren und Triphenylen geben. - 3.4-Benzpyren liefert unter milden Bedingungen das 5-Brom-Derivat VII. Weitere Chlorierung von Trichlor-3.4-benzpyren VIII führt zum Trichlor-3.4-benzpyren-tetrachlorid IX.
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  • 83
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 249-254 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Produkte des Zerfalls der 1.2-Benzo-cyclenyl-(4)-diazonium-lonen (II) in Essigsäure werden mit denen der Acetolyse der 1.2-Benzo-cyclenyl-(4)-tosylate (VI) verglichen. Die erste Reaktion vollzieht sich am Beispiel des Vertreters mit 7-gliedrigem Ring mit 53-proz., die zweite mit 89-proz. Konfigurationserhaltung.
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  • 84
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 282-284 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thioschwefelsäure läß sich mit Thionylchlorid in guten Ausbeuten unter Chlorwasserstoffabspaltung zu einem äquimolaren Gemisch aus Disulfan-disulfonsäure und Trisulfan-disulfonsäure oxydieren. Mit Sulfurylchlorid bildet H2S2O3 neben HCI und Schwefeldioxid reine H2S4O6.
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  • 85
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 285-294 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 4.5.8-Trihydroxy-6-mercapto-chinolin-carbonsäure-(2) (II) wird durch Spaltung des Xanthogenats XV mit Aluminiumbromid dargestellt. Die Spaltung von XV mit Bromwasserstoffsäure führt zur reduktiven Abspaltung der Schwefelfunktion. Bei der Methylierung von II mit Diazomethan entsteht neben dem vollmethylierten Chinolinderivat XXI ein Chinolon XXII, bei dem die zur Chinolon-Carbonylgruppe peri-ständige 5-Hydroxygruppe unmethyliert bleibt. II ist wider Erwarten nicht identisch mit einem aus dem Ommochrom „Ommin A“ dargestellten Abbauprodukt.
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  • 86
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 300-301 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 87
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 307-311 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei der Oxydation von Pyrogallol in alkoholischer Lösung wird Purpurogallincarbonsäure-(9)-ester gebildet, dessen Konstitution sich aus dem Abbau zu Purpurogallin und Methylterephthalsäure ergibt.
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  • 88
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 312-324 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1′.2′-Dihydroxy-benzotropolon-Derivate können nach zwei Methoden dargestellt werden: 1.aus 3 Moll. eines o-Benzochinons mit unsubstituierter Doppelbindung und 1 Mol. eines geeigneten Pyrogallolderivates, 2. durch Oxydation eines Gemisches geeigneter Brenzcatechin- und Pyrogallolderivate mit KJO3 bzw. K3[Fe(CN)6]. Bei der Umsetzung von o-Benzochinonen mit 4-Methylpyrogallol wird nur dasjenige Isomere (I a) gebildet, bei welchem die Reaktionspartner im Orientierungskomplex die räumlich günstigste Anordnung (Methylgruppe auf der von der Verknüpfungsstelle abgewandten Seite) haben. Zwei Synthesen für Trimethylpyrogallol und die Darstellung von 2′-Hydroxy-benzotropolon-chinon-(1′.4′) (VIII) werden beschrieben.
    Additional Material: 2 Tab.
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  • 89
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 349-362 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: symm. Tetra-pyrenyl-(3)-äthan (III), symm. Di-pyrenyl-(3)-diphenyl-äthan (VII), 2.3-Di-[pyrenyl-(3)]-butan (IX), 2.2.5.5-Tetramethyl-3.4-diphenyl-3.4-di-[pyrenyl-(3)]-hexan (X) und Hexa-pyrenyl-(3)-äthan (XI) wurden dargestellt und ihre Fähigkeit zur Dissoziation in Radikale bei Raumtemperatur mit Hilfe der Elektronenspinreasonanz -Method (ESR) untersucht. Mit Ausnahme von 2.3-Di-[pyrenyl-(3)]-butan sind sämtliche der untersuchten Verbindungen bei Raumtemperatur partiell, das Hexa-[pyrenyl-(3)]-äthan erwartungsgemäß quantitativ dissoziiert. Beim symm. Tetra-α-naphthyl-äthan (VIII) ist dagegen keine Radikaldissoziation nachweisbar. - Das von Pyren ausgehend in guter Ausbeute in zweistufiger Synthese darstellbare symm. Tetra-pyrenyl-(3)-äthan ist im organischen Solvens bei Raumtemperatur unlöslich. Es ist im festen Zustand zu 0.0025% in Radikale dissoziiert. - Die Abhängigkeit der Carbonylfrequenz im IR-Spektrum von Mono- und Diarylderivaten des Formaldehyds vom Kondensationsgrad des Arylrestes wurde untersucht.
    Additional Material: 3 Tab.
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  • 90
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 390-395 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 3-Halogen-pyridazine reagieren mit Anthranilsäure oder Anthranilsäure-äthyl-ester zu Pyridazino[3.2-b ]chinazolonen-(10), deren Eigenschaften beschrieben werden.
    Additional Material: 1 Tab.
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  • 91
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 382-389 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei Eliminierung des Chlors aus cis-3.4-Dichlor-cyclobuten mittels Natriumamalgam in äther. Lösung entsteht das syn-Tricyclo[4.2.0.02.5]octadien-(3.7) (I), identisch mit dem früher aus 1.2.3.4-Tetrabrom-cyclobutan erhaltenen Produkt. Bei ähnlicher Behandlung mit Lithiumamalgam bildet sich überwiegend das isomere anti- Tricycloocatadien (II). Die Ozonspaltung und einige Derivate dieser Kohlenwasserstoffe werden beschrieben.
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  • 92
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 415-418 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Umsetzung von L-Tryptophan mit D-Fructose liefert kristallisierte 2-Nα-L-Tryptophan-2-desoxy-D-glucose(I), mit D-Glucose 1-Nα-L-Tryptophan-1-desoxy-D-fructose (II), Aus L-Histidin und D-Fructose entsteht 2-Nα-L-Histidin-2-desoxy-D-Glucose (II).
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  • 93
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 426-432 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei der Umsetzung der Hexacarbonyle der Chromgruppe mit Bipyridyl-(2.2′) bzw. 1.10-Phenanthrolin geht die Substitution über die Tetracarbonylstufen M(CO)4bipy bzw. M(CO)4phen hinaus, wenn man in hochsiedenden Kohlenwasserstoffen, wie Decalin, Tetralin oder 1-Methyl-naphthalin arbeitet. Während mit Mo(CO6 und W(CO)6 die Dicarbonylverbindungen M(CO)2bipy2 bzw. M(CO)2phen2 gebildet werden, entstehen mit Cr(CO)6 die totalsubstituierten Typen Cr(bipy)3 und Cr(phen)3.
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  • 94
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Hexacarbonyle M(CO)6 (M=Cr, Mo, W) setzen sich bei 120° mit flüssigem NH3 zu den Tricarbonyltriamminverbindungen M(CO)3(NH3)3 um; nur beim Cr(CO) 6 ist bei 80° auch Cr(CO)5NH3 zugänglich. Bei den Reaktionen von M(CO)4bipy und M(CO)4phen (bipy = Bipyridyl-(2.2′), phen = 1.10-Phenanthrolin) mit flüssigem NH3 erfolgt bei 120° Substitution einer CO-Molekel unter Bildung der Verbindungstypen M(CO)3 bipyNH3 bzw. M(CO)3phenNH3. Bei den Umsetzungen von M(CO)4bipy mit Kaliumcyanid in flüssigem NH3 wird bei 60° bipy vollständig durch CN⊖ ersetzt. Hierbei werden mit Cr(CO)4bipy K2[Cr0(CO) 4(CN)2], mit Mo(CO)4bipy und W(CO)4bipy unter gleichzeitiger CO-Substitution K3[M0(CO) 3(CN)3] gebildet.
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  • 95
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 472-479 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aryl- und Alkylisocyanate reagieren mit Benzolderivaten unter Friedel-Crafts-Bedingungen zu N-substituierten Benzoesäureamiden. Auch die wenig reaktionsfähigen Halogenbenzole sind der Umsetzung zugänglich.
    Additional Material: 6 Tab.
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  • 96
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 563-565 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Das kürzlich als 2-Hydroxy-4.5-epoxy-6-O-methyl-tetrahydro-apogalanthamin beschriebene Abbauprodukt aus Galanthamin wurde als (-)-Epigalanthamin identifiziert.
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  • 97
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 579-587 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Wegen der zentralen Stellung der Chinonmethide in der Chemie des Lignins wurden 3 niedermolekulare p-Chinonmethide auf ihre chemischen Reaktionen und ihre Polymerisation untersucht. Die Polymerisate sind zur monomeren Stufe abzubauen und bestehen aus fortlaufend verätherten p-Hydroxy- benzyl-alkoholen (Polybenzylaryläthern) vom Typus XX.
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  • 98
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 602-609 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die cis-Formen geometrischer Isomerenpaare scheinen ganz allgemein energie ärmer zu sein, wenn nicht H-H-Wechselwirkung oder extreme Raumbeanspruchung wie beim 1.2-Dijod-äthylen vorliegen. Die Isolierung der geometrischen Isomeren der im Titel genannten Verbindungen erlaubt deren Strukturzuordnung und die Untersuchung der thermischen Gleichgewichte. Die cis-cis-Isomeren sind in Benzollösung energetisch gegenüber den trans-trans-Isomeren stark bevorzugt, welche bei den Meßtemperaturen von 100° und 150° nur zu 10 bis 15% im Gleichgewicht vertreten sind.
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  • 99
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Messungen der Optischen Rotationsdispersion und des Zirkulardichroismus von N-Phthalyl-aminen beweisen die Existenz von mindestens einer optischaktiven Absorptionsbande im Bereich oberhalb von 300 mμ, die im UV-Spektrum nicht erkennbar ist. Aus dem Vorzeichen der zugehörigen Cotton-Effekt-Kurve kann die absolute Konfiguration bestimmt werden: N-Phthalyl-Derivate optisch-aktiver Amine der (R)-Reihe zeigen einen negativen Cotton-Effekt, solche der (S)-Reihe einen positiven. Entsprechende Messungen an N-Phthalyl-Derivaten von α-Aminosäuren führten zum Nachweis von mindestens zwei optischaktiven Absorptionsbanden, die wiederum im UV-Spektrum nicht erkennbar sind. Die vorliegende Untersuchung stellt ein weiteres Beispiel dar für die Anwendung der Optischen Rotationsdispersion und besonders des Zirkulardichroismus zur Ermittlung verdeckter Absorptionsbanden.
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  • 100
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    Berichte der deutschen chemischen Gesellschaft 97 (1964), S. 566-574 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bei Versuchen, Cyanformaldehyd herzustellen, wurden bei Raumtemperatur nur Cyanwasserstoff und Kohlenmonoxyd bzw. Ameisensäure erhalten. Dagegen konnten das Oxim und Phenylhydrazon des Cyanformaldehyds, beide in syn- und anti- Form, dargestellt werden. Das Cyanformaldoxim ist extrem unbeständig gegen Basen, die den exothermen Zerfall in Dicyan und Wasser katalysieren. Das Oxim und Phenylhydrazon sowie geeignete Derivate konnten nicht zu Abkömmlingen des s-Triazin-trialdehyds trimerisiert werden.
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