Heinz Falk

Infobox Person
name = Heinz Falk

---

image_size = 180px
caption = Heinz Falk
nationality = AUT
residence= Linz, Austria
birth_date = birth date and age|1939|04|29
birth_place = Sankt Pölten, Austria
death_date =
death_place =
occupation = Professor emeritus
spouse = Rotraud Falk, (1966-present)
parents =
children = Alexander Falk

Heinz Falk (born April 29, 1939 in Sankt Pölten, Austria) is professor emeritus for organic chemistry at Johannes Kepler University of Linz,
editor of "Progress in the Chemistry of Organic Natural Compounds" [ [http://www.springer.com/series/126 Springer Wien/New York, Progress in the Chemistry of Organic Natural Compounds] ] , and editor-in-chief of "Chemical Monthly". [ [http://www.springer.com/springerwiennewyork/chemistry/journal/706?detailsPage=editorialBoard Springer Wien/New York, Chemical Monthly, Editorial Board] ] His research is focused on structural analysis, synthesis, stereochemistry and photochemistry of plant and animal photosensitizing and photosensory pigments, such as hypericin. [http://www.orc.uni-linz.ac.at/falk/falk.html Hypericin Group at the Institute of Organic Chemistry] ]

Biography

Early life

Heinz Falk was born April 29, 1939 in Sankt Pölten, Austria, went to elementary school in Statzendorf and completed middle school in Krems an der Donau. After moving to Vienna in 1953 he completed a three-year program at [http://www.htl17.at/ HBLVA for Chemical Industry, Rosensteingasse] and completed his high-school diploma in 1959 through classes at an evening school, where he met his future wife, Rotraud Falk (née Strohbach).

Marriage and children

Heinz Falk is married to Rotraud Falk since 1966 and they have one son:
*Alexander Falk (August 13, 1967) is the CEO of Altova.

Education

Heinz Falk studied chemistry at the University of Vienna starting in 1959 and completed his dissertation under his doctoral advisor, Karl Schlögl, in 1966. In 1971 Falk spent a year abroad to study at ETH Zürich. Upon his return to Vienna in 1972 he attained habilitation for organic chemistry at the University of Vienna.

Career

1966-1979: University of Vienna
Starting in 1966 Falk was an assistant at the [http://www.univie.ac.at/orgchem/ Institute of Organic Chemistry] at the University of Vienna. In 1975 he was promoted to associate professor of physical organic chemistry at the University of Vienna. In the summer of 1978 Falk was invited to speak at the Gordon Research Conference in Wolfeboro.
1979-present: Johannes Kepler University of Linz
In 1979 Falk received a call to become full professor of organic chemistry at Johannes Kepler University of Linz, where he founded the new [http://www.orc.uni-linz.ac.at/ Institute of Organic Chemistry] . From 1989 through 1991 he was elected Dean of the Faculty of Engineering and Natural Sciences ( [http://www.tn.jku.at/ TNF] ) at Johannes Kepler University of Linz. In 2005 Falk was ranked #3 among the "Top 10" scientists in Upper Austria by the newspaper "OÖ Nachrichten". [http://www.nachrichten.at/bestofooe/395099 OÖ Nachrichten - Best of OÖ Teil 18: Die klügsten Köpfe] ]

Research interests

Falk's main research area is the structural analysis, synthesis, stereochemistry and photochemistry of plant and animal photosensitizing and photosensory pigments. The main group of compounds covered in his work are pigments derived from the fundamental phenanthro [1,10,9,8-opqra] perylene-7,14-dione chromophore with natural pigments like hypericin, stentorin, the fringelites, the gymnochromes, and blepharismin. In addition, he is focusing on hemin-analogous corrphycene derivatives (e.g. as potential blood substitutes and heme oxygenase blocker) as well as on other natural compounds such as the natural sun blocker urocanic acid. Furthermore, research on applied problems of industrial relevance, like oxidation, ozonization, non natural amino acids and catalysis have been pursued.

Published works

Books

*cite book | last = Falk | first = Heinz | title = Ausgewählte Übungsbeispiele Zur Nomenklatur Organischer Verbindungen | publisher = Springer-Verlag | location = Wien, New York| year = 1978 | isbn = 0387814795
*cite book | last = Falk | first = Heinz | title = The Chemistry of Linear Oligopyrroles and Bile Pigments | publisher = Springer-Verlag | location = Wien, New York| year = 1989 | isbn = 0387821120

cientific Articles

*H. Marko, N. Müller und H. Falk, Nuclear Magnetic Resonance Investigations of the Biliverdin/Apomyoglobin Complex. Eur. J. Biochem. 193, 573 (1990)
*H. Falk, H. Marko, N. Müller, W. Schmitzberger und H. Stumpe, Reconstitution of Apomyoglobin with Bile Pigments. Monatsh. Chem. 121, 893 (1990)
*H. Falk, H. Marko, N. Müller und W. Schmitzberger, On the Chemistry of Pyrrole Pigments 87.Mitt.: The Apomyoglobin Heme Pocket as a Reaction Vessel in Bile Pigment Chemistry. Monatsh. Chem. 121, 903 (1990)
*H. Falk und H. Marko, Reduction of a Bilindione-10-Thiol-Adduct as a Model for the Reduction Step of the Biliverdin Reductase System. Monatsh. Chem. 122, 319 (1991)
*U. Wagner, C. Kratky, H. Falk und H. Woess, Crystal Structure and Conformation of 10-Aryl-bilatrienes-abc. Monatsh. Chem. 122, 749 (1991)
*H. Falk und G. Schoppel, A Synthesis of Emodin Anthrone. Monatsh. Chem. 122, 739 (1991)
*H. Falk and W. Schmitzberger, On the Nature of "Soluble" Hypericin in Hypericum Species. Monatsh. Chem., 123, 731 (1992)
*H. Falk and D. Hemmer, On the Chemistry of Pyrrole Pigments, 88. Mitt.: Nonlinear Optical Properties of Linear Oligopyrroles. Monatsh. Chem. 123, 779 (1992)
*H. Falk and G. Schoppel, On the Synthesis of Hypericin by Oxidative Trimethylemodin Anthrone and Emodin Anthrone Dimerization: Isohypericin. Monatsh. Chem. 123, 931 (1992)
*H. Falk and W. Schmitzberger, On the Bromination of Hypericin: The Gymnochrome Chromophores. Monatsh. Chem. 124, 77 (1993)
*C. Etzlstorfer, H. Falk, N. Müller, W. Schmitzberger and U. Wagner, Tautomerism and Stereochemistry of Hypericin: Force Field, NMR, and X-ray Crystallographic Investigations. Monatsh. Chem., 124, 751 (1993)
*H. Falk and A. Suste, On the Chemistry of Pyrrole Pigments, XC: Pyridinologous Linear Tri- and Tetrapyrroles. Monatsh. Chem., 124, 881 (1993)
*H. Falk, J. Meyer and M. Oberreiter, A Convenient Semisynthetic Route to Hypericin. Monatsh. Chem., 124, 339 (1993)
*C. Etzlstorfer and H. Falk, Tautomerism and Stereochemistry of Isohypericin, Bromo-hypericines, and Gymnochromes: Force Field Investigations. Monatsh. Chem., 124, 1031 (1993)
*H. Pschierer, J. Friedrich, H. Falk and W. Schmitzberger, On the Correlation Between Pressure Shift and Solvent Shift: A Spectral Hole Burning Study. J. Phys. Chem., 97, 6902 (1993)
*A. Angerhofer, H. Falk, J. Meyer and G. Schoppel, The Lowest Triplet States of Hypericin and Isohypericin. J. Photochem. Photobiol., B20, 133 (1993)
*H. Falk and A. Suste, On the Chemistry of Pyrrole Pigments, XCI: Copper Complexes of Pyridinologous Linear Tri- and Tetrapyrroles as Cyclopropanation Catalysts. Monatsh. Chem., 125, 325 (1994)
*H. Falk and J. Meyer, On the Homo- and Heteroassociation of Hypericin. Monatsh. Chem., 125, 753 (1994)
*C. Etzlstorfer and H. Falk, Stereochemistry and Tautomerism of Stentorin, Isostentorin, and Fringelit D: Force Field Investigations. Monatsh. Chem., 125, 955 (1994)
*H. Falk, E. Mayr and A. Richter, Simple Diffuse Reflectance UV-Vis Spectroscopic Determination of Organic Pigments (Fringelites) in Fossils. Microchim. Acta, 117, 1 (1994)
*H. Falk and J. Leimhofer, Ozone as an Oxygen Source for Alkene Ene-Reactions. Monatsh. Chem., 126, 85 (1995)
*Q.-Q. Chen, H. Falk and R. Micura, On the Chemistry of Pyrrole Pigments, XCII: Syntheses of 1,2-Bis-pyrrolylethanes. Monatsh. Chem., 126, 473 (1995)
*H. Falk, C. Kratky, N. Müller, W. Schmitzberger and U. Wagner, Structure Determination of the Biliverdin Apomyoglobin Complex. Crystal Structure Analysis of Two Crystal Forms at 1.4 and 1.5 * Resolution. J. Mol. Biol., 247, 326 (1995)
*N. H. Tran-Thi and H. Falk, An Efficient Synthesis of the Plant Growth Hormone 1-Triacontanol. Monatsh. Chem., 126, 565 (1995)
*H. Falk and A. F. Vaisburg, Concerning the Absorption and Emission Properties of Phenanthro [1,10,9,8,o,p,q,r,a] perylene-7,14-dione. Monatsh. Chem., 126, 361 (1995)
*H. Falk and E. Mayr, Syntheses and Properties of Fringelite D (1,3,4,6,8,10,11,13-octahydroxy-phenanthro [1,10,9,8,o,p,q,r,a] perylene-7,14-dione). Monatsh. Chem., 126, 699 (1995)
*H. Falk, A.F. Vaisburg and A.M. Amer, On the Synthesis of w-Appended Hypericin Derivatives. Monatsh. Chem., 126, 993 (1995)
* R. Altmann and H. Falk, On the Syntheses and Chiroptical Properties of the Tri- and Tetragalloylquinic Acids. Monatsh. Chem. 126, 1225 (195)
* D. Shemin and H. Falk, Porphyrins and Bile Pigmens, Metabolism Encyclopedia of Human Biology, 2nd Ed., Academic Press, 177 (1996)
* H. Falk and Q.-Q. Chen, On the Chemistry of Pyrrole Pigments, XCVI: An Efficient Synyhesis of Corrphycenes. Mh. Chem., 127, 69 (1996)
* H. Falk and E. Mayr, Syntheses, Constitutions, and Properties of Stentorin and Isostentorin. Mh. Chem., 126, 1311 (1995)
* H. Falk and T.N.H. Tran, Synthesis and Properties of an w,wÕ - Appended Eighteen Carbon Chains Hypericin Derivative. Mh. Chem., 127, 717 (1996)
*C. Etzlstorfer, H. Falk, N. Müller and T.N.H. Tran, Structural Aspects and Electronic Absorption of the Hydroxyphenanthroperylene Quinones Fringelit D, Hypericin, and Stentorin. Mh. Chem., 127, 659 (1996)
*C. Etzlstorfer, H. Falk, E. Mayr and S. Schwarzinger, Concerning the Acidity and Hydrogen Bonding of Hydroxyphenantroperylene Quinones, like Fringelite D, Hypericin, and Stentorin. Mh. Chem., 127,1229 (1996)
*R. Altmann, C. Etzlstorfer and H. Falk, Chiroptical Properties and Absolute Configurations of the Hypericin Chromophore Propeller Enantiomers. Mh. Chem., 128, 785 (1997)
*H. Falk and M. Stanek, Two-Dimensional 1H and 13C NMR Spectroscopy and the Structural Aspects of Amylose and Amylopectin. Mh. Chem., 128, 777 (1997)
*H. Falk, A.A.O. Sarhan, H.T.N. Tran and R. Altmann, Synthesis and Properties of Hypericins Substituted with Acidic and Basic Residues: Hypericin Tetrasulfonic Acid – a Water Soluble Hypericin Derivative. Mh. Chem., 129, 309 (1998)
*E.I. Kapinuns, H. Falk and T.N.H. Tran, Spectroscopic Investigaion of the Molecular Structures of Hypericin and its Salts. Mh. Chem., 130, 1237 - 1244 (1999)
*A.M. Amer, H. Falk, H.N.T. Tran, The Dissociation and Tautomerization Equilibria of Hypericin: Alkyl Protected Hydroxyl Derivatives. Mh. Chem., 130, 623 - 635 (1999)
*R. Obermüller, G. Schütz, H. Gruber and H. Falk, Concerning Regioselective Photochemical Intermolecular Proton Transfer from Hypericin. Mh. Chem., 130, 275 - 281 (1999)
*G. Kada, H. Falk and H. Gruber, Accurate Measurement of Avidin and Streptavidin in Crude Biofluids with a New, Optimized Biotin. Fluorescein Conjugate. Biochim. Biophys. Acta, 1427, 33 - 43 (1999)
*C. Etzlstorfer, I Gutman and H. Falk, Concerning the Deprotonation ot the Photooxidized 3-Hypericinate Ion. Mh. Chem., 130, 1333 - 1339 (1999)
*T. Dax, H. Falk and E. Kapinus, A Structural Proof for the Hypericin 1,6-Dioxo Tautomer. Mh. Chem., 130, 827 - 831 (1999)
*H. Falk, Gosau Schleifsteine fuer den Fossiliensammler. Fossilien, 4, 248 - 250 (1999)
*H. Falk, Vom Photosensibilisator Hypericin zum Photorezeptor Stentorin - die Chemie der Phenanthroperylenchinone. Angew. Chemie, 111, 3306 - 3326 (1999)
*H. Falk, From the Photosensibilisator Hypericin to the Photoreceptor Stentorin - the Chemistry of the Phenanthroperylene Quinones. Angew. Chemie Int. Ed., 38, 3134 - 3154 (1999)
*S. Baumgartner, T. Dax, W. Praznik and H. Falk, Characterization of the high-molecular weight fructan isolated from garlic (Allium sativum L.). Carbohydrate Res., 328, 177-183 (2000)
*C. Etzlstorfer and H. Falk, Concerning the Association of Hypericin Tautomers and their Hypericinate Ions. Mh. Chem., 131, 333-340 (2000)
*T. Dax, E. Kapinus and H. Falk, A Remarkable Photoreaction of 3-O-Benzylhypericin. Helvetica Chimica Acta, 83, 1744-1752 (2000)
*B. Immitzer, C. Etzlstorfer, R. Obermüller, M. Sonnleitner, G. Schütz, and H. Falk, On the Photochemical Proton Expulsion Capability of Fringelite D — A Model of the Protist Photosensory Pigments of the Stentorin and Blepharismin Types. Mh. Chem., 131, 1039-1045 (2000)
*T. Dax, C. Etzlstorfer, and H. Falk, On the Ground State Energy Hypersurface of Blepharismins and Oxyblepharismins. Mh. Chem., 131, 1115-1122 (2000)
*B. Immitzer and H. Falk, Fringelite D, a Model of the Protist Photosensory Pigments of the Stentorin and Blepharismin Types: the Hypericin and Fringelite D Photosensitized Destruction of Bilirubin. Mh. Chem., 131, 1167-1171 (2000)
*T. Dax and H. Falk, An Unusual Photoreaction of 3,4,-Di-O-benzyl-hypericin. Mh. Chem., 131, 1217-1219 (2000)
*E. Delaey, R. Obermüller, I. Zupko, H. Falk, and P. de Witte, In vitro Study of the Photocytotoxicity of some Hypericin analogs on different Cell Lines. Photochem. Photobiol., 74, 164-171 (2001)
*R.A. Obermüller, K. Hohenthanner, and H. Falk, Towards Hypericin-Derived Potential Photdynamic Therapy Agents. Photochem. Photobiol., 74, 211-215 (2001)
*B. Tu, Q. Chen, F. Yan, J. Ma, K. Grubmayr, and H. Falk, Efficient Routes to -Chloroalkyl Bilirubins and C12-N22 Bridged Biliverdins. Mh. Chem., 132, 693-705 (2001)
*R.A. Obermüller, T. Dax and H. Falk, Replacement of Methoxy- to tert-Butyl-Substitution on a Napththalene Residue – An Unexpected Reaction Observed During a Snieckus ortho-Lithiation. Mh. Chem., 132, 1057-1062 (2001)
*R.A. Obermüller and H. Falk, Concerning the Absorption and Photochemical Properties of an -4-Dimethylaminobenzal Hypericin Derivative. Mh. Chem., 132, 1519-1526 (2001)
*R.A. Obermüller, C. Etzlstorfer and H. Falk, On the Chemistry of a Dibenzohypericin Derivative. Mh. Chem., 133, 89-96 (2002)
*J. Leonhartsberger and H. Falk, The Protonation and Deprotonation Equilibria of Hypericin Revisited. Mh. Chem., 133, 167-172 (2002)
*B. Lackner and H. Falk, Concerning the Diastereomerization of Stilbenoid Hypericin Derivatives. Mh. Chem., 133, 717-721 (2002)
*T.N. Tran and H. Falk, Concerning the Chiral Discrimination and Helix Inversion Barrier in Hypericinates and Hypericin Derivatives. Mh. Chem., 133, 1231-1237 (2002)
*M. Emsenhuber, P. Pöchlauer, J.-M. Aubry, V. Nardello and H. Falk, Evidence for the Generation of Singlet Oxygen (1O2, 1g) from Ozone Promoted by Inorganic Salts. Mh. Chem., 133, 387-391 (2003)
*M. Deak and H. Falk, On the Chemistry of the Resveratrol Diastereomers. Mh. Chem., 134, 883-888 (2003)
*T.A. Salama, B. Lackner and H. Falk, An Efficient Synthesis of O-Methyl Protected Emodin Aldehyde and Emodin Nitrile. Mh. Chem., 134, 1113-1119 (2003)
*Bettina Schwarzinger, and Heinz Falk, A Unique Photoreaction of Hypericinate Bound to Human Serum Albumin, Lipids, or Vesicles. Mh. Chem., 134, 1353-1358 (2003)
*Beate Hager, Mario Alva-Astudillo, and Heinz Falk, A Hemin-Analogous Corrphycene Derivative: Suppression of Heme Oxygenase and Reconstitution with Apomyoglobin. Mh. Chem., 134, 1499-1507 (2003)
*Tarek A. Salama, Bernd Lackner, and Heinz Falk, Synthesis of 6-Heterocyclically Appendend Tri-O-Methyl Protected 6-Desmethyl Emodin Derivatives. Mh. Chem., 135, 735-742 (2004)
*Thorsten Ganglberger, Walther G. Jary, Peter Pöchlauer, Jean-Marie Aubry, Veronique Nardello, and Heinz Falk, A Chemical (Dark) Source of Singlet Oxygen: Ozone Splitting Promoted by Tin(II) Salts. Mh. Chem., 135, 501-507 (2004)
*Walther G. Jary, Thorsten Ganglberger, Peter Pöchlauer, and Heinz Falk, Generation of Singlet Oxyen from Ozone Catalysed by Phosphinofer-rocenes. Mh. Chem., 136, 537-541 (2005)
*Bernd Lackner, Christoph Etzlstorfer and Heinz Falk, Synthesis and Properties of 10,11-Dibenzimidazolyl-10,11-didesmethyl-hypericin – The First Heterocyclically Substituted Hypericin Derivative. Mh. Chem., 135, 1157-1166 (2004)
*Bettina Schwarzinger and Heinz Falk, Concerning the Photodiastereomerization and Protic Equilibria of Urocanic Acid and its Complex with Human Serum Albumin. Mh. Chem., 135, 1297-1304 (2004)
*Mario Waser, Heinz Falk, Peter Pöchlauer and Walther G. Jary, Concerning Chemistry, Reactivity, and Mechanism of Transition Metal Catalysed Oxidation of Benzylic Compounds by Means of Ozone. Journal of Molecular Catalysis A - Chemical, , 236, 187-193 (2005)
*Mario Waser and Heinz Falk, Intramolecularly Friedel-Crafts Acylated Emodin Derivatives: An Access to the Cores of Angucyclinones, Anthracyclinones, and to Hypericin Analogues. Mh. Chem., 136, 609-618 (2005)
*Bernd Lackner, Yulita Popova, Christiph Etzlstorfer, Andrija A. Smelcerovic, Christian W. Klampfl, and Heinz Falk, Syntheses and Properties of Two Heterocyclically Substituted Hypericin Derivatives: 10,11-Dibenzothiazolyl-10,11-didesmethyl-hypericin and 10,11-Dibenzoxazolyl-10,11-didesmethylhypericin. Mh. Chem., 136, 777-793 (2005)
*Mario Waser, Bernd Lackner, Joachim Zuschrader, Norbert Müller, and Heinz Falk, An efficient regioselective synthesis of endocrocin and structural related natural anthraquinones starting from emodin. Tetrahedron Lett., 46, 2377-2380 (2005)
*Bernd Lackner, Klaus Bretterbauer, and Heinz Falk, An Efficient Route to Emodic Amine and Analogous O-Methyl Protected Derivatives Starting from Emodin. Mh. Chem., 136, 1629-1639 (2005)
*Mario Waser, Yulita Popova, Christoph Etzlstorfer, Werner F. Huber, and Heinz Falk, Syntheses, Photochemical Properties, and Tautomerism of Intramolecularly Friedel-Crafts Acylated Hypericin Derivatives. Mh. Chem., 136, 1221-1231 (2005)
*David Geißlmeir, Walther G. Jary and Heinz Falk, The TEMPO/Copper Catalyzed Oxidation of Primary Alcohols to Aldehydes Using Oxygen as Stoichometric Oxidant. Mh. Chem., 136, 1591-1599 (2005)
*Mario Waser, Yulita Popova, Christian W. Klampfl, and Heinz Falk, 9,12-Dibenzothiazolylhypericin and 10,11-Dibenzothiazolyl-10,11-Didemethylhypericin: Photochemical Properties of Hypericin Derivatives Depending on the Substitution Site. Mh.Chem., 136, 1791-1797 (2005)
*Klaus Wolkenstein, Jürgen H. Gross, Heinz Falk, and Heinz F. Schöler, Preservation of hypericin and related polycyclic quinone pigments in fossil crinoids. Proceedings of the Royal Society B, 273, 451-456 (2006)
*Beate Hager, Bettina Schwarzinger and Heinz Falk, Concerning the Thermal Diastereomerization of the Green Fluorescent Protein Chromophore. Mh. Chem., 137, 163-168 (2006)
*Mario Waser and Heinz Falk, Condensed Emodin Derivatives and Their Applicability for the Synthesis of a Fused Heterocyclic Hypericin Derivative. Eur. J. Org. Chem., 1200-1206 (2006)
*Mario Waser and Heinz Falk, Towards Second Generation Hypericin Based Photosensitizers for Photodynamic Therapy. Curr. Org. Chem. 11: 547-558 (2007)
*Heinz Falk: Karl Schlögl. Obituary. Mh. Chem., 138 (2007)
*Karoline Fendler, Beate Hager, and Heinz Falk, The Thermal Diastereomerization of the Tryptophane-Derived Green Fluorescent Protein Chromophore. Mh. Chem., 138, 859-862 (2007)
*Mieke Roelants, Heinz Falk, Bernd Lackner, Mario Waser, Peter A.M. de Witte, OC222 Bathochromically shifted hypericin derivatives: photosensitizing properties. Abstr. of 12th Congress of the Europaean Society for Photobiology 2007, University of Bath, UK, Sept 1/6, (2007)
*Heinz Falk, Die 44. Mineralientage München - ein Rückblick. Fossilien, 25, 2-4 (2008)
*Heinz Falk. Karl Schlögl, Nachruf. Almanach d. Öst. Akademie der Wiss. , 157, 469-477 (2008)

Patents

* [http://www.google.com/patents?id=l5wdAAAAEBAJ&dq=ininventor:%22heinz+falk%22&as_drrb_
] US Pat. 5124451 - Filed Jul 10, 1991 - Chemie Linz GmbH
* [http://www.google.com/patents?id=va8fAAAAEBAJ&dq=ininventor:%22heinz+falk%22&as_drrb_
] US Pat. 5169954 - Filed Dec 16, 1991 - Chemie Linz GmbH
* [http://www.google.com/patents?id=K7ccAAAAEBAJ&dq=ininventor:%22heinz+falk%22&as_drrb_
] US Pat. 5283362 - Filed Jul 31, 1992 - Chemie Linz GmbH
* [http://www.google.com/patents?id=XU4aAAAAEBAJ&dq=5360601 Process for the preparation of Isocyanic Acid by Decomposition of N,N-trisubstituted Ureas] Eur. Pat. EP 0582863A2 - Filed Feb 16, 1994 - US Pat. Nr. 5360601 Filed Nov 1, 1994 - Chemie Linz GmbH
*"Isocyanates by Decomposition of N,N,N-trisubstituted Ureas" Eur. Pat. EP 0583637A1 - Filed Feb 23, 1994 - Chemie Linz GmbH
* [http://www.google.com/patents?id=XBUbAAAAEBAJ&dq=ininventor:%22heinz+falk%22&as_drrb_
] US Pat. 5409532 - Filed Jan 21, 1993 - Lenzing AG

Awards

*Theodor Körner Prize for Science and Art in Austria, 1970
*Ernst Späth Prize of the Austrian Academy of Sciene, 1976
*Sandoz Prize, 1977
*Election to "corresponding member" of the New York Academy of Sciences, 1989
*Election to "corresponding member" of the Mathematical and Natural Sciences Class of the Austrian Academy of Sciences, 1992
*Upper Austrian Prize for Science, 1993
*Election to "full member" of the Mathematical and Natural Sciences Class of the Austrian Academy of Sciences, 1997 [ [http://www.oeaw.ac.at/english/about/personen/mitglieder.html Austrian Academy of Sciences, Academy Members] ] [ [http://www.news.jku.at/Portale/NvC/NvC_content/content/e1703/e1711/ausgabe22.pdf Johannes Kepler University - News vom Campus, Ausgabe 22, March 2004] ]
*Josef Loschmidt Medal of the Austrian Chemical Society, 1998 [ [http://www.goech.at/HallOfFame/loschmidt_en.shtml Austrian Chemical Society, Hall of Fame] ]
*Election as member of the European Academy of Sciences, 2003 [ [http://www.oeaw.ac.at/oeaw_servlet/e_PersonenDetailsGeneric?id=10874 Austrian Academy of Sciences, Member details] ]
*Scientifc award of the Rudolf Trauner Stiftung, 2003 [http://portal.wko.at/wk/sn_detail.wk?AngID=1&DocID=178394 Rudolf Trauner Stiftung, Scientific Awards 2003] ]

References

;General
* [http://www.orc.uni-linz.ac.at/falk/falk.html Hypericin Group at the Institute of Organic Chemistry, Johannes-Kepler University Linz] ;Specific

See also

* Hypericin
* Organic chemistry
* Physical organic chemistry
* Johannes Kepler University of Linz
* University of Vienna

External links

* [http://www.orc.uni-linz.ac.at/falk/falk.html Hypericin Group at the Institute of Organic Chemistry]
* [http://www.orc.uni-linz.ac.at/ Institute of Organic Chemistry]
* [http://www.jku.at/ Johannes-Kepler University, Linz, Austria]

References

Persondata
NAME=Falk, Heinz
ALTERNATIVE NAMES=
SHORT DESCRIPTION=Professor emeritus of Organic Chemistry, Johannes-Kepler University Linz
DATE OF BIRTH=April 29 1939
PLACE OF BIRTH=Sankt Pölten
DATE OF DEATH=
PLACE OF DEATH=