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Title of Journal: Monatsh Chem

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Abbravation: Monatshefte für Chemie - Chemical Monthly

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Springer Vienna

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DOI

10.1007/bf00518749

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1434-4475

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Editorial

Authors: Peter Gärtner
Publish Date: 2009/09/16
Volume: 140, Issue: 10, Pages: 1137-1138
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Abstract

As some of you may have realized at the end of October 2008 the EditorinChief Prof Heinz Falk and with him all other Editors resigned due to problems which were solved in May 2009 Whereas the other Editors continued with their duties then Prof Heinz Falk who was operating as EditorinChief since 1998 decided not to come back Thus a new EditorinChief had to be assigned and I was in May 2009 nominated by the Austrian Academy of Science and the Austrian Chemical Society both owners of Monatshefte für Chemie/Chemical Monthly After a short time of consideration and a brief talk with my friend Prof Falk who promised to support me as much as possible I accepted the nominationIt was of course an honor to become EditorinChief but it was certainly not an easy decision to take this position Anybody who knows Prof Falk more well will confirm that Monatshefte für Chemie/Chemical Monthly was like a “child” for him that he cared for with a great deal of personal effort I think I can judge this at least to some extent because I have had very close contacts with him since 2003 when I became Editorial Assistant/Managing Editor Anyway it is difficult to measure this personal effort but as an indication of what he did for the journal let us have a brief look at the development of the impact factor of the journal under his guidance When he became EditorinChief in 1998 the impact factor of Monatshefte für Chemie/Chemical Monthly was around 05 and after a continuous increase during the period he guided the journal it was nearly 15 for the year 2008 Although we all are aware of problems in connection with impact factors Prof Falk himself does not believe that they are a valid instrument to quantify the scientific quality of a journal or a paper if published in this journal for several reasons that I cannot replicate here they are still used in the scientific community If we use them to compare the development of the Monatshefte für Chemie/Chemical Monthly I dare say what he did for the journal cannot be overestimated and the footprints he is leaving are really big Thus I would feel a bit uncomfortable as his successor if I had to do this job without his assistance but as mentioned above Prof Falk offered his helping hands and I am counting on himOf course a journal with about 1500 pages a year covering all areas of chemistry cannot be handled by only one Editor and thus part of the success is also due to the members of the Editorial Board who I am more than happy to welcome back They have supported Prof Falk fantastically and I hope that they will do so for me as wellLast but not least a scientific journal would be nothing without the contributions from its authors Thus a big part if not the biggest of the success is also due to this group The more interesting the submitted papers are the more resonance they will generate and this will of course influence the impact factor positively I hope to welcome back most of you but also young scientists publishing for the first time are invited to submit their most important papersTo further increase the speed of processing during the last Editorial Board meeting it was decided to appoint two additional editors It is therefore my particular pleasure to welcome Prof Jürgen Fleig Physical Chemistry Vienna University of Technology and Prof Wolfgang Buchberger Analytical Chemistry Johannes Kepler University Linz to the Board I hope that they will enjoy their tasks as do all the other members of the Board and support us as much as possible in our endeavorFinally I wish for all of us that we can proceed with our journal on the path that Prof Falk paved and be as successful as he was in maintaining high standards In this regard I would like to mention two particular points First I think that we should continue with our Special Issues focused on current trends in chemistry such as we recently had on topics like “Solid state ionics electrochemistry meets material science” “Sensor devices and biosensors in food analysis” “From molecules to molecular devices” “Computational chemistry” “Ionic liquids—a survey of recent developments and applications” etc All of them have given very detailed insight into selected areas of research in these fields but can also be recommended as broad overviews to scientists moving into these subjects Proposals for such Special Issues are always welcome and I am convinced that they will also be a successThe second point I would like to mention at the very end because I feel that this is an important argument and I want it to be recognized is the ownership of Monatshefte für Chemie/Chemical Monthly by both the Austrian Chemical Society and the Austrian Academy of Science two organizations representing Austrian scientists Although the journal is nowadays an international one with contributions from all over the world I think it would be appropriate also to have more submissions from Austrian scientists again I would go so far to say it should be a moral obligation for all chemistry scientists in Austria in the broadest sense to submit some of their best scientific achievements to Monatshefte für Chemie/Chemical Monthly As the development of the impact factor in the last couple of years has shown it can change significantly if the quality of submissions is good and this is the accomplishment of our authorsFor my new position I am looking forward to a prosperous development of our journal to good collaboration with all Editors and to a large number of topquality submissions on contemporary research from our authors and then I think the future of Monatshefte für Chemie/Chemical Monthly will be brilliant This is all it needs


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  1. Revised Phase Diagram of the System NaF–NaBF 4
  2. Highly efficient three-component, one-pot synthesis of dihydropyrano[3,2- c ]chromene derivatives
  3. Synthesen von isomeren Methyl- und 1,1′-Dimethylferrocencarbonsäuren
  4. DFT molecular orbital calculations and natural bond orbital analysis of 1,2,7-thiadiazepane conformers
  5. Complexation of Li + with antamanide: an experimental and theoretical study
  6. Cyclic α -amino acids as precursors for synthesis of 2-amino-3-hetarylpyrrolin-4-ones and their spiro derivatives
  7. 7,15-Diazadispiro[5.1.5.3]hexadecan und Derivate, 1. Mitt.: Darstellung der Grundkörper
  8. Reaching for cyclacenes and short nanotubes through Si substitutions as studied by DFT calculations
  9. Über Dialkylidensulfamide
  10. Spectrometric methods for determination of ligand–protein ratio in monoclonal conjugates: a mini review
  11. Carbon–nitrogen nanorings and nanoribbons: a theoretical approach for altering the ground states of cyclacenes and polyacenes
  12. Methylendiformamid: Ausgangsmaterial für oligomere Carbonsäureamide und-imide
  13. The scale-up of material microstructuring: from scanning probes to self-assembly
  14. 4th Young Investigator Workshop
  15. Mittlere Schwingungsamplituden der Seleninylhalogenide
  16. Amino Acid Derivatives, VII [1]: Synthesis and Antiviral Evaluation of α-Amino Acid Esters Bearing an Indazole Side Chain
  17. Intramolecular Diels–Alder cyclization of biodihydroxylated benzoic acid derivatives towards novel heterocyclic scaffolds
  18. Stereoselektive Synthese einiger Amidester der (±)-erythro-2,3-Diphenylglutarsäure
  19. Regioselective synthesis of 3,5-diaryl-4-methylisoxazoles
  20. The Willgerodt-Kindler Reaction in Water: High Chemoselectivity of Benzaldehydes over Acetophenones
  21. Beitrag zur Kenntnis des Systems Vanadin—Chrom—Stickstoff
  22. Direct injection mass spectrometry, thin layer chromatography, and gas chromatography of Bacillus subtilis phospholipids
  23. Thermodynamic data for lanthanoid(III) sequestration by phytate at different temperatures
  24. Isocyanide-based one-pot three-component synthesis of novel spiroiminolactone derivatives in water
  25. Theoretical study of cation–π interactions of Li + , Na + , and K + with [6]helicene
  26. Phthalimide- N -oxyl salts: efficient organocatalysts for facile synthesis of ( Z )-3-methyl-4-(arylmethylene)-isoxazole-5(4 H )-one derivatives in water
  27. Synthesis, Analgesic, and Antiparkinsonian Profiles of Some Pyridine, Pyrazoline, and Thiopyrimidine Derivatives
  28. Expedient approach for the synthesis of novel indenothiophene derivatives
  29. Nitroacetylene as dipolarophile in [2 + 3] cycloaddition reactions with allenyl-type three-atom components: DFT computational study
  30. Synthesis of 3-(quinoxalin-2-yl)-2 H -chromen-2-ones under microwave irradiation
  31. Exploring the Limits of Emulsion Polymerization of Styrene for the Synthesis of Polymer Nanoparticles
  32. Reaktionen von Organometallverbindungen, 3. Mitt.: Zur Kinetik der Reaktionen von Tetraorganoplumbanen mit Essigsäure
  33. Diastereoselective syntheses of ( Z )- and ( E )-3-styrylquinolin-4(1 H )-ones
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  35. Switching central trinucleotide sequences of DNA heptamer regulates adsorption on mercury electrode
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  37. Phase relations in the Nb–Ni–Cr system at 1,100 °C
  38. Preparation of an improved sulfonated carbon-based solid acid as a novel, efficient, and reusable catalyst for chemoselective synthesis of 2-oxazolines and bis-oxazolines
  39. Synthesis, characterization, and anticancer properties of ferrocenyl complexes containing a salicylaldehyde moiety
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  41. Synthesis of a C-2 Stapled Bis-Lexitropsin
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  43. Zur Darstellung von Imidazolidin-thionen-(4) und Imidazolin-(3)-thionen-(5)
  44. Alkoxycarbonylpiperidines as N-nucleophiles in the palladium-catalyzed aminocarbonylation

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