Relevant bibliographies by topics / Halogen molecule

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Halogen molecule'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Halogen molecule"

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Hirama, Atsuki, Shohei Yoshinaga, Naoki Shida, and Mahito Atobe. "Electrochemical C-N Bond Formation Reaction by Using the Halogen Bond Interaction of Haloanthracene and Its Kinetic Analysis." ECS Meeting Abstracts MA2025-01, no. 48 (2025): 2470. https://doi.org/10.1149/ma2025-01482470mtgabs.

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Halogens in organic compounds are usually regarded as electron-rich due to their high electronegativity. However, it is known that the electron density of halogen atoms with covalent bonds is anisotropically distributed. Specifically, the negative electrostatic potential is distributed perpendicular to the covalent bond, while the positive electrostatic potential emerges along the extension of the bond. This electron-deficient region, called as σ-hole, becomes larger as the halogen atoms increase in their size, and it forms a non-covalent interaction called a halogen bond with nucleophilic mol
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Zhang, Yu, Jian-Ge Wang, and Weizhou Wang. "Noncovalent Interactions between 1,3,5-Trifluoro-2,4,6-triiodobenzene and a Series of 1,10-Phenanthroline Derivatives: A Combined Theoretical and Experimental Study." Crystals 9, no. 3 (2019): 140. http://dx.doi.org/10.3390/cryst9030140.

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How many strong C−I⋯N halogen bonds can one 1,3,5-trifluoro-2,4,6-triiodobenzene molecule form in a crystal structure? To answer this question, we investigated in detail the noncovalent interactions between 1,3,5-trifluoro-2,4,6-triiodobenzene and a series of 1,10-phenanthroline derivatives by employing a combined theoretical and experimental method. The results of the quantum chemical calculations and crystallographic experiments clearly show that there is a structural competition between a C−I⋯N halogen bond and π⋯π stacking interaction. For example, when there are much stronger π⋯π stacking
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Saccone, Marco, Giancarlo Terraneo, Tullio Pilati, et al. "Azobenzene-based difunctional halogen-bond donor: towards the engineering of photoresponsive co-crystals." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 70, no. 1 (2013): 149–56. http://dx.doi.org/10.1107/s205252061302622x.

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Halogen bonding is emerging as a powerful non-covalent interaction in the context of supramolecular photoresponsive materials design, particularly due to its high directionality. In order to obtain further insight into the solid-state features of halogen-bonded photoactive molecules, three halogen-bonded co-crystals containing an azobenzene-based difunctional halogen-bond donor molecule, (E)-bis(4-iodo-2,3,5,6-tetrafluorophenyl)diazene, C12F8I2N2, have been synthesized and structurally characterized by single-crystal X-ray diffraction. The crystal structure of the non-iodinated homologue (E)-b
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Akkurt, Mehmet, Abel Maharramov, Namig Shikhaliyev, et al. "Crystal structure and Hirshfeld surface analysis of (E)-1-(4-chlorophenyl)-2-(2,2-dibromo-1-(3-nitrophenyl)vinyl)diazene." UNEC journal of engineering and applied sciences 3, no. 1 (2023): 33–39. http://dx.doi.org/10.61640/ujeas.2023.0506.

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The molecule of the title compound, C14H8Br2ClN3O2, consists of three almost planar groups: the central dibromoethenyldiazene fragment and two attached aromatic rings. The mean planes of these rings form dihedral angles with the plane of the central fragment of 17.00 (13) and 60.91 (13)0 for chlorine- and nitro-substituted rings, respectively. In the crystal, face-to-face π-π stacking interactions connect molecules in zig-zag chains along the a-axis. With halogen⋅⋅⋅halogen, halogen⋅⋅⋅hydrogen, Br⋅⋅⋅H, O⋅⋅⋅H, N⋅⋅⋅H and van der Waals interactions between these chains, molecular packing becomes s
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Moreno-Fuquen, Rodolfo, Alexis Azcárate, and Alan R. Kennedy. "4-Bromo-N-(2-nitrophenyl)benzamide." Acta Crystallographica Section E Structure Reports Online 70, no. 3 (2014): o344. http://dx.doi.org/10.1107/s1600536814003298.

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The title nitrophenyl benzamide, C13H9BrN2O3, with two molecules in the asymmetric unit, has dihedral angles of 16.78 (15) and 18.87 (14)° between the benzene rings. An intramolecular N—H...O hydrogen bond is observed in each molecule. In the crystal, the molecules are linked by weak C—H...O interactions; halogen–halogen interactions are also observed [Br...Br = 3.4976 (7) Å]. These interactions formR22(10),R22(15) andR66(32) edge-fused rings along [010].
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Raner, K. D., J. Lusztyk, and K. U. Ingold. "Ultraviolet/visible spectra of halogen molecule/arene and halogen atom/arene .pi.-molecular complexes." Journal of Physical Chemistry 93, no. 2 (1989): 564–70. http://dx.doi.org/10.1021/j100339a016.

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Şerb, Mihaela-Diana, Carina Merkens, Irmgard Kalf та Ulli Englert. "Halogen bonds on demand: I...S contacts in cocrystals oftrans-bis(thiocyanato-κN)tetrakis(4-vinylpyridine-κN)nickel(II) and 2,3,5,6-tetrafluoro-1,4-diiodobenzene". Acta Crystallographica Section C Structural Chemistry 71, № 11 (2015): 991–95. http://dx.doi.org/10.1107/s2053229615019002.

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Hydrogen bonds are considered a powerful organizing force in designing supramolecular architectures because they are directional, selective and reversible at room temperature.trans-Dithiocyanatotetrakis(4-vinylpyridine)nickel(II) is a popular host for the inclusion of small molecules and 2,3,5,6-tetrafluoro-1,4-diiodobenzene (TFDIB) represents a strong halogen-bond donor. These constituents cocrystallize in a 1:1 stoichiometry, [Ni(NCS)2(C7H7N)4]·C6F4I2, in the tetragonal space groupI41/a. Both residues occupy special positions,i.e.the pseudo-octahedral NiIIcomplex is located on a twofold axis
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Vijayakumar, S., Duminda S. Ranasinghe, and David M. Wilmouth. "Kinetics of the Reactions of Ozone with Halogen Atoms in the Stratosphere." Atmosphere 12, no. 8 (2021): 1053. http://dx.doi.org/10.3390/atmos12081053.

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It is well established that reaction cycles involving inorganic halogens contribute to the depletion of ozone in the atmosphere. Here, the kinetics of O3 with halogen atoms (Cl, Br, and I) were investigated between 180 and 400 K, expanding the temperature range relative to prior studies. Canonical variational transition state theory including small curvature tunneling correction (CVT/SCT) were considered, following the construction of the potential energy surfaces. MRCI + Q/aug-ano-pVTZ//MP2/aug-cc-pV(T + d)Z and MRCI + Q/aug-ano-RCC-VTZP//MP2/aug-cc-pV(T + d)Z levels of theory were used to ca
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Hamilton, Victoria, Connah Harris, Charlie L. Hall, et al. "Structural effects of halogen bonding in iodochalcones." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 77, no. 3 (2021): 347–56. http://dx.doi.org/10.1107/s2052520621002961.

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The structures of three iodochalcones, functionalized with fluorine or a nitro group, have been investigated to explore the impact of different molecular electrostatic distributions on the halogen bonding within each crystal structure. The strongly withdrawing nitro group presented a switch of the halogen bond from a lateral to a linear motif. Surprisingly, this appears to be influenced by a net positive shift in charge distribution around the lateral edges of the σ-hole, making the lateral I...I bonding motif less preferable. A channel of amphoteric I...I type II halogen bonds is observed for
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Varadwaj, Pradeep, Arpita Varadwaj, and Helder Marques. "Halogen Bonding: A Halogen-Centered Noncovalent Interaction Yet to Be Understood." Inorganics 7, no. 3 (2019): 40. http://dx.doi.org/10.3390/inorganics7030040.

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In addition to the underlying basic concepts and early recognition of halogen bonding, this paper reviews the conflicting views that consistently appear in the area of noncovalent interactions and the ability of covalently bonded halogen atoms in molecules to participate in noncovalent interactions that contribute to packing in the solid-state. It may be relatively straightforward to identify Type-II halogen bonding between atoms using the conceptual framework of σ-hole theory, especially when the interaction is linear and is formed between the axial positive region (σ-hole) on the halogen in
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Dissertations / Theses on the topic "Halogen molecule"

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Wilson, Philip John. "Potential energy curves of halogen molecule ion-pair states." Thesis, University of Edinburgh, 1994. http://hdl.handle.net/1842/14689.

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The double resonance ionisation nozzle cooled spectroscopy technique (DRINCS) has been used to extend the existing vibrational constants for some ion-pair states of I<SUB>2</SUB> and IC1. Some new ion-pair states of IC1 have also been observed. Some ion-pair potential energy curves beyond the previously existing RKR potentials have been generated using only the vibrational Dunham coefficients and the known asymptotic behaviour of the Coulombic branch of the potentials of I<SUB>2</SUB>. These potentials have been used to simulate the DRINCS spectra. The lifetime of the f'(v'=0) ion-pair state o
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Vulpe, Elena. "Molecular tectonics based on fluorinated porphyrins." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAF048/document.

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Les travaux décrits dans ce manuscrit utilisent les principes de la tectonique moléculaire pour générer des polymères de coordination hautement fluorés et /ou chiraux pour une application potentielle en séparation chirale. La synthèse de 13 porphyrines de type A2B2 substituées en position méso par deux pyridines et par deux chaines fluorées et/ou alkyles a été mise au point. Des réseaux de coordination ont été obtenus en présence de Zn(II) et de Cd(II) et caractérisés par diffraction des RX sur monocristal (DRX). Une analyse systématique des interactions supramoléculaires et notamment de inter
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Salama, Farid. "Etude de la photoexcitation dans l'ultra-violet lointain des halogènes piégés en matrice de gaz rare à basse température et étude de leur ionisation simple et double par impact protonique en phase gazeuse." Paris 6, 1986. http://www.theses.fr/1986PA066213.

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I. Etude des mécanismes de relaxation mis en jeu dans Cl2, Br2, I2 isolés en matrice, après excitation en UV proche ou lointain : émission structurée (transitions vibroniques) pour Cl2en UV proche et transitions électroniques avec interaction Rydberg-Valence en UV lointain; émission dans le visible pour Br2 et I2 quelle que soit l'énergie d'excitation; étude théorique des processus de relaxation. II. Observation d'ions moléculaires simplement ou doublement chargés, formés par échange de charge simple ou double étudié par spectrométrie de translation; analyse des règles de sélection : conservat
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Flexen, Alexander C. "Vacuum ultraviolet laser spectroscopy of diatomic halogen and interhalogen molecules." Thesis, University of Edinburgh, 1999. http://hdl.handle.net/1842/13824.

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The Rydberg and ion-pair states of Cl<SUB>2</SUB>, Br<SUB>2</SUB>, I<SUB>2</SUB>, ICl and IBr have been studied using a range of laser-based spectroscopic techniques, in the vacuum-ultraviolet (VUV) energy region. The [2+1] resonance enhanced multiphoton ionization (REMPI) spectrum of Br<SUB>2</SUB> has been re-examined in the region 56 000-86 000 cm<SUP>-1</SUP>. Rydberg series, previously assigned to components of the <I>ns</I> Rydberg states have been reassigned to components of the (<I>n</I>-2)d Rydberg states, for <I>n</I>≥6. The lowest 5s Rydberg state components on each ionic core remai
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Lim, Jason Yuan Chong. "Halogen and chalcogen bonding host molecules for anion recognition and sensing." Thesis, University of Oxford, 2017. https://ora.ox.ac.uk/objects/uuid:e1eb91e7-d635-40a9-aea5-6bbf9bedb56b.

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This thesis describes the preparation and study of acyclic, macrocyclic and mechanicallyinterlocked host molecules (MIMs) exploiting halogen and chalcogen bonding interactions for anion recognition and sensing. <b>Chapter 1</b> introduces the field of anion supramolecular chemistry and interlocked structures, with emphasis on halogen and chalcogen bonding receptors, as well as their applications in catalysis, molecular recognition and nanotechnology. <b>Chapter 2</b> explores the methodology development and synthesis of novel neutral and cationic macrocyclic and interlocked host molecules cont
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Mereshchenko, Andrey S. "ULTRAFAST PHOTOCHEMISTRY OF POLYATOMIC MOLECULES CONTAINING LABILE HALOGEN ATOMS IN SOLUTION." Bowling Green State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1369774991.

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GONDA, R. DE. "MODELING OF MOLECULAR INTERACTIONS: FROM PROTEIN-PROTEIN TO HALOGEN BOND." Doctoral thesis, Università degli Studi di Milano, 2014. http://hdl.handle.net/2434/244525.

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Part I - Microtubules are polymeric structures formed by the self association of tubulin dimers. They are extremely dinamical structures, that can undergo phases of growing and shrinking, playing a key role during cells proliferation process. Due to its importance for mitosis, tubulin is the target of many anticancer drugs currently in use or under clinical trial. The success of these molecules, however, is limited by the onset of resistant tumor cells during the treatment, so new resistance-proof compounds need to be developed. We analyze the protein-protein interactions betwee
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Halonen, Maria. "Monogenic model for autoimmune diseases : molecular basis of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)." Helsinki : University of Helsinki, 2003. http://ethesis.helsinki.fi/julkaisut/laa/haart/vk/halonen/.

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Fedchak, James Anthony. "Collisions of atomic hydrogen with oxygen, sulfur, sodium and halogen anions at low energies." W&M ScholarWorks, 1994. https://scholarworks.wm.edu/etd/1539623856.

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Total electron detachment and charge transfer cross sections, $\sigma\sb{\rm e}$(E) and $\sigma\sb{\rm ct}$(E), have been measured for collisions of the negative ions O$\sp{-}$, S$\sp{-}$, F$\sp{-}$, Cl$\sp{-}$, Br$\sp{-}$, I$\sp{-}$, Na$\sp{-}$, and K$\sp{-}$ with atomic hydrogen for laboratory energies ranging from 2 to 500 eV. For the systems F$\sp{-}$, Cl$\sp{-}$, Br$\sp{-}$, O$\sp{-}$ and S$\sp{-}$ + H, $\sigma\sb{\rm e}$(E) displays no barrier for associative detachment; the results are found to be adequately described by simple curve-crossing models based upon available intermolecular p
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Rosano, William Joseph. "Chemiluminescence and laser induced fluorescence of the group IVA and IB elements with halogen molecules /." The Ohio State University, 1985. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487263399026961.

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Books on the topic "Halogen molecule"

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Metrangolo, Pierangelo, and Giuseppe Resnati. Halogen Bonding: Fundamentals and Applications. Springer, 2010.

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Metrangolo, Pierangelo, and Giuseppe Resnati. Halogen Bonding: Fundamentals and Applications. Springer London, Limited, 2008.

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Metrangolo, Pierangelo, and Giuseppe Resnati. Halogen Bonding I: Impact on Materials Chemistry and Life Sciences. Springer International Publishing AG, 2016.

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Chemistry, Royal Society of. Halogen Bonding in Supramolecular and Solid State Chemistry: Faraday Discussion 203. Royal Society of Chemistry, The, 2017.

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Metrangolo, Pierangelo, and Giuseppe Resnati. Halogen Bonding I: Impact on Materials Chemistry and Life Sciences. Springer, 2015.

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Metrangolo, Pierangelo, and Giuseppe Resnati. Halogen Bonding I: Impact on Materials Chemistry and Life Sciences. Springer London, Limited, 2015.

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Metrangolo, Pierangelo, and Giuseppe Resnati. Halogen Bonding II: Impact on Materials Chemistry and Life Sciences. Springer, 2015.

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Metrangolo, Pierangelo, and Giuseppe Resnati. Halogen Bonding II: Impact on Materials Chemistry and Life Sciences. Springer London, Limited, 2015.

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Metrangolo, Pierangelo, and Giuseppe Resnati. Halogen Bonding II: Impact on Materials Chemistry and Life Sciences. Springer International Publishing AG, 2016.

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Hudlic'ky, Milos. Fluorine Chemistry for Organic Chemists. Oxford University Press, 2000. http://dx.doi.org/10.1093/oso/9780195131567.001.0001.

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This book is a synthesis of two of Hudlicky's earlier books outlining the many unpredictable properties of fluorine and its compounds that are not analogous to the properties of any other halogens and their compounds. It is divided into two separate sections, the first presenting peculiar reactions as problems to be solved. Each reaction can be analyzed in the lab without the help of the second section, however if a solution is not easily reached, the second section provides discussion of the problems, outlining the products of the reactions and their mechanisms. Among the 105 reactions outlin
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Book chapters on the topic "Halogen molecule"

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Pang, Yui Tik. "Parameterization of a Drug Molecule with a Halogen $$\sigma $$-Hole Particle Using ffTK: Implementation, Testing, and Comparison." In Springer Theses. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-70602-8_2.

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Noorbatcha, I., B. Arifin, and S. M. Zain. "Ab Initio Quantum Chemical Studies of Six-Center Bond Exchange Reactions Among Halogen and Halogen Halide Molecules." In Computational Science – ICCS 2007. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-72586-2_48.

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Tognetti, Vincent, and Laurent Joubert. "Following Halogen Bonds Formation with Bader’s Atoms-in-Molecules Theory." In Challenges and Advances in Computational Chemistry and Physics. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29022-5_16.

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Kurita, Susumu. "Polarons and Solitons in Halogen-Bridged Platinum Complexes: Effects of Photoexcitation and Halogen-Doping on Optical Absorption and Esr Spectra." In Lower-Dimensional Systems and Molecular Electronics. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-2088-1_29.

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Costa, Paulo J. "Transmembrane Anion Transport Mediated by Halogen Bonds: Using Off-Center Charges." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1468-6_16.

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Becker, Kurt H. "Electron Impact Induced Dissociative Excitation and Ionization of Halogen-Containing Molecules." In Electron Collisions with Molecules, Clusters, and Surfaces. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-1489-7_10.

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Kelley, D. F., and N. A. Abul Haj. "Geminate Recombination and Relaxation of Condensed Phase Molecular Halogens." In Springer Series in Chemical Physics. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82918-5_89.

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Song, Wentao, and Anthony M. Granville. "Surface Modification of Polydivinylbenzene Microspheres with a Fluorinated Glycopolymer Using Thiol-Halogen Click Chemistry." In Methods in Molecular Biology. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3130-9_10.

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Mínguez Espallargas, Guillermo. "Supramolecular Interactions and Smart Materials: C-X…X′-M Halogen Bonds and Gas Sorption in Molecular Solids." In Ideas in Chemistry and Molecular Sciences. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527630530.ch5.

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Cline, Joseph I., Dwight D. Evard, Brian P. Reid, N. Sivakumar, Fritz Thommen, and Kenneth C. Janda. "Structure and Dynamics of the Rare Gas-Halogen Van Der Waals Molecules: Product State Distributions for Vibrational Predissociation of NeBr2." In Structure and Dynamics of Weakly Bound Molecular Complexes. Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3969-1_39.

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Conference papers on the topic "Halogen molecule"

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Meier, Daniel, and Andrew Xie. "Development of a New Yellow Metal Corrosion Inhibitor." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-12770.

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Abstract This paper will outline the development of a new Yellow Metal corrosion inhibitor with improved corrosion control capabilities when compared to traditional triazole technology. A four-year R&amp;D effort has led to a new patent pending molecule that develops a thicker, more robust film, greatly reducing the impact of high levels of halogen on the corrosion of copper and copper alloy heat transfer surfaces. This paper will outline laboratory corrosion testing and film formation and finally field applications.
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Wang, Xuejun, Andrew (Yanjiao) Xie, James Michels, and Donald Johnson. "Corrosion Inhibition Mechanism Study of a Novel Yellow Metal Corrosion Inhibitor." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-12847.

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Abstract The corrosion inhibition mechanism of a new yellow metal corrosion inhibitor was studied using multiple characterization techniques including ellipsometry, white light interferometry (WLI), grazing incidence reflection absorption Fourier transform infrared (GIRA-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS) and high-performance liquid chromatography (HPLC). Compared to traditional azole molecules, the novel yellow metal corrosion inhibitor develops a stimuli-responsive film, which would reduce the impact of high levels of halo
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Chu, Po-Tao, Ching-Wen Cho, Hung-Chi Hsiao, Jie-Shin Wu, Chih-Chien Hung, and Ying-Chen Chao. "Characterization of environmental halogen molecule contamination-induced pad surface corrosion." In Microelectronic Manufacturing, edited by Ali Keshavarzi, Sharad Prasad, and Hans-Dieter Hartmann. SPIE, 1997. http://dx.doi.org/10.1117/12.284704.

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GRANTIER, D., H. WANG, C. WINSTEAD, and J. GOLE. "Chemically driven continuous visible laser amplifiers and oscillators based on molecule-halogen atom reactions." In 24th Plasma Dynamics, and Lasers Conference. American Institute of Aeronautics and Astronautics, 1993. http://dx.doi.org/10.2514/6.1993-3207.

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Abrams, M. C., M. R. Gunson, A. Y. Chang, C. P. Rinsland, R. Zander, and M. H. Newchurch. "Validation of Stratospheric Ozone Observed by the Atmospheric Trace Molecule Spectroscopy (ATMOS) Experiment During 1992." In Optical Remote Sensing of the Atmosphere. Optica Publishing Group, 1995. http://dx.doi.org/10.1364/orsa.1995.wc5.

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Measurements of stratospheric ozone were made by the Atmospheric Trace Molecule Spectroscopy (ATMOS) experiment from onboard the Space Shuttle during the period 8-16 April 1992. The precision and accuracy of the measurements are discussed in the context of establishing the accuracy and compatibility of the measurements relative to other space-based measurements of ozone. Coincident measurements were obtained from the Stratospheric Aerosol and Gas Experiment (SAGE) II instrument onboard the Earth Radiation Budget Satellite (ERBS) and three instruments, the Microwave Limb Sounder (MLS), the Cryo
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Kepeňová, Martina, Michaela Benediková, Mária Vilková, Miroslava Litecká, and Ivan Potočňák. "Ionic palladium(II) complexes with nitro and halogen derivatives of 8-hydroxyquinoline." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.443k.

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Four commercially unavailable derivatives of 8-hydroxyquinoline with different functional groups (nitro and halogen) in positions 5 and 7 were prepared: 5-nitro-7-iodo-8-hydroxyquinoline (HNIQ), 5-nitro-7-bromo-8-hydroxyquinoline (HNBrQ), 5-iodo-7-bromo-8-hydroxyquinoline (HIBrQ) and 5-chloro-7-bromo-8-hydroxyquinoline (HClBrQ). Their characterization was performed by IR and NMR spectroscopy, elemental analysis and in the case of HIBrQ and HClBrQ by single crystal X-ray structure analysis. Prepared compounds were used for the synthesis of new palladium(II) complexes NH2(CH3)2[PdCl2(XQ)], where
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Buchachenko, Alexei A., and N. F. Stepanov. "Calculations of spectra and dynamics of rare-gas halogen molecule complexes using the semi-empirical potential energy surfaces." In 12th Symposium and School on High Resolution Molecular Spectroscopy, edited by Leonid N. Sinitsa, Yurii N. Ponomarev, and Valery I. Perevalov. SPIE, 1997. http://dx.doi.org/10.1117/12.267790.

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Gunson, M. R., M. C. Abrams, C. B. Farmer, L. L. Lowes, C. P. Rinsland, and R. Zander. "Results from the flight of the Atmospheric Trace Molecule Spectroscopy on the ATLAS-1 Space Shuttle Mission." In Optical Remote Sensing of the Atmosphere. Optica Publishing Group, 1993. http://dx.doi.org/10.1364/orsa.1993.ma.4.

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During the ATLAS-1 space shuttle mission, the ATMOS experiment, a Fourier transform infrared spectrometer operating in solar occultation mode from on-orbit (Farmer, 1987), collected data through more than 90 orbital sunrises and sunsets at latitudes between 30°N and 55°S. The resulting high-resolution infrared solar absorption spectra from these observations have so far been analyzed for the vertical profiles of several species (O3, HNO3, ClNO3, HCl, HF, N2O, CH4 and H2O) of immediate importance as correlative measurements for other satellite instruments, such as those carried on the Upper Atm
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Zdravković, Nemanja, Milan Ninković, Ivan Pavlović, et al. "Quaternary ammonium compounds." In 36. Savetovanje dezinfekcija, dezinsekcija i deratizacija jedan svet - jedno zdravlje, Vrnjačka Banja, hotel "Vrnjačke Terme", 28-31.maj 2025.godine. Srpsko veterinarsko društvo, 2024. https://doi.org/10.5937/ddd25015z.

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Next to their positive role, microorganisms are associated with numerous undesirable effects, including many diseases, food spoilage, and decay. Humanity have been combating microorganisms for centuries. It was observed that water could be carried on long journeys in silver containers or with silver or copper coins, and food was preserved using salt and/or spices. In the modern era, the use of phenol as a disinfectant is well-known. The term "biocides" refers to a group of chemical compounds whose primary purpose is the deactivation or destruction of vegetative microorganisms. Due to their bio
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Lotshaw, William T., Dale McMorrow, and Geraldine A. Kenney-Wallace. "Femtosecond laser spectroscopy studies of electronic nonlinearities in the halogen substituted benzenes." In OSA Annual Meeting. Optica Publishing Group, 1987. http://dx.doi.org/10.1364/oam.1987.thr11.

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The femtosecond time-resolved optical Kerr effect (OKE) in room temperature polyatomic molecular liquids contains a wealth of information on the dynamics and structure of molecules through their nonlinear optical susceptibility.1 We present new femtosecond time-resolved results on the OKE of liquid benzene, nitrobenzene, and the series of monohalogenated benzenes (F, Cl, Br, I) which demonstrate the influence of the substituent (NO2 or halogen) on the purely electronic hyperpolarizability of these molecules.
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