Intermolecular Forces
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Periodic Table and Bonding Notes 2
Periodic Table and Bonding 1. Handout: Periodic Table and Bonding Notes 2. Periodic Properties and the Development of the Periodic Table 1. The first periodic table was arranged by Dimitri Mendeleev in 1869. 1. He was a professor of Chemistry. at the University of St. Petersburg in Russia and was confronted with the problem of how to teach about the various elements known at that time. He decided to organized the elements by arranging them into groups that reacted similarly. 2. He also noticed that various properties would repeat "periodically" so he arranged a table of elements order of atomic mass such that properties would change regularly if you moved across a row while maintaining groups with similar chemical properties in a column. 3. Go to: http://www.periodic.lanl.gov/mendeleev.htm to see a version of Mendeleev's first table. 2. Groups with similar properties 1. All the elements in a group (or column) are called families. 2. Group 8: The Noble Gases, don't react with other elements. 3. Group 1: The Alkali Earth Metals, all react with water in the following manner 2 Li + H2O ---> H2 + 2 LiOH 2 Na + H2O ---> H2 + 2 NaOH ... 2 Fr + H2O ---> H2 + 2 FrOH page 1 4. These are just a few examples of how Mendeleev organized the columns or families. 3. Periodic Properties 1. As you move across a row various properties change regularly click on the images below to see a visualization of the various properties. All of these images are from www.webelements.com, one of the best periodic table sites on the web. -
Topological Analysis of the Metal-Metal Bond: a Tutorial Review Christine Lepetit, Pierre Fau, Katia Fajerwerg, Myrtil L
Topological analysis of the metal-metal bond: A tutorial review Christine Lepetit, Pierre Fau, Katia Fajerwerg, Myrtil L. Kahn, Bernard Silvi To cite this version: Christine Lepetit, Pierre Fau, Katia Fajerwerg, Myrtil L. Kahn, Bernard Silvi. Topological analysis of the metal-metal bond: A tutorial review. Coordination Chemistry Reviews, Elsevier, 2017, 345, pp.150-181. 10.1016/j.ccr.2017.04.009. hal-01540328 HAL Id: hal-01540328 https://hal.sorbonne-universite.fr/hal-01540328 Submitted on 16 Jun 2017 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Topological analysis of the metal-metal bond: a tutorial review Christine Lepetita,b, Pierre Faua,b, Katia Fajerwerga,b, MyrtilL. Kahn a,b, Bernard Silvic,∗ aCNRS, LCC (Laboratoire de Chimie de Coordination), 205, route de Narbonne, BP 44099, F-31077 Toulouse Cedex 4, France. bUniversité de Toulouse, UPS, INPT, F-31077 Toulouse Cedex 4, i France cSorbonne Universités, UPMC, Univ Paris 06, UMR 7616, Laboratoire de Chimie Théorique, case courrier 137, 4 place Jussieu, F-75005 Paris, France Abstract This contribution explains how the topological methods of analysis of the electron density and related functions such as the electron localization function (ELF) and the electron localizability indicator (ELI-D) enable the theoretical characterization of various metal-metal (M-M) bonds (multiple M-M bonds, dative M-M bonds). -
Introduction to Aromaticity
Introduction to Aromaticity Historical Timeline:1 Spotlight on Benzene:2 th • Early 19 century chemists derive benzene formula (C6H6) and molecular mass (78). • Carbon to hydrogen ratio of 1:1 suggests high reactivity and instability. • However, benzene is fairly inert and fails to undergo reactions that characterize normal alkenes. - Benzene remains inert at room temperature. - Benzene is more resistant to catalytic hydrogenation than other alkenes. Possible (but wrong) benzene structures:3 Dewar benzene Prismane Fulvene 2,4- Hexadiyne - Rearranges to benzene at - Rearranges to - Undergoes catalytic - Undergoes catalytic room temperature. Faraday’s benzene. hydrogenation easily. hydrogenation easily - Lots of ring strain. - Lots of ring strain. - Lots of ring strain. 1 Timeline is computer-generated, compiled with information from pg. 594 of Bruice, Organic Chemistry, 4th Edition, Ch. 15.2, and from Chemistry 14C Thinkbook by Dr. Steven Hardinger, Version 4, p. 26 2 Chemistry 14C Thinkbook, p. 26 3 Images of Dewar benzene, prismane, fulvene, and 2,4-Hexadiyne taken from Chemistry 14C Thinkbook, p. 26. Kekulé’s solution: - “snake bites its own tail” (4) Problems with Kekulé’s solution: • If Kekulé’s structure were to have two chloride substituents replacing two hydrogen atoms, there should be a pair of 1,2-dichlorobenzene isomers: one isomer with single bonds separating the Cl atoms, and another with double bonds separating the Cl atoms. • These isomers were never isolated or detected. • Rapid equilibrium proposed, where isomers interconvert so quickly that they cannot be isolated or detected. • Regardless, Kekulé’s structure has C=C’s and normal alkene reactions are still expected. - But the unusual stability of benzene still unexplained. -
Symmetry of Three-Center, Four-Electron Bonds†‡
Chemical Science EDGE ARTICLE View Article Online View Journal | View Issue Symmetry of three-center, four-electron bonds†‡ b a c Cite this: Chem. Sci., 2020, 11,7979 Ann Christin Reiersølmoen, § Stefano Battaglia, § Sigurd Øien-Ødegaard, Arvind Kumar Gupta, d Anne Fiksdahl,b Roland Lindh a and Mate Erdelyi *a All publication charges for this article ´ ´ ´ have been paid for by the Royal Society of Chemistry Three-center, four-electron bonds provide unusually strong interactions; however, their nature remains ununderstood. Investigations of the strength, symmetry and the covalent versus electrostatic character of three-center hydrogen bonds have vastly contributed to the understanding of chemical bonding, whereas the assessments of the analogous three-center halogen, chalcogen, tetrel and metallic s^-type long bonding are still lagging behind. Herein, we disclose the X-ray crystallographic, NMR spectroscopic and computational investigation of three-center, four-electron [D–X–D]+ bonding for a variety of cations (X+ ¼ H+,Li+,Na+,F+,Cl+,Br+,I+,Ag+ and Au+) using a benchmark bidentate model system. Formation of a three-center bond, [D–X–D]+ is accompanied by an at least 30% shortening of the D–X Received 11th April 2020 bonds. We introduce a numerical index that correlates symmetry to the ionic size and the electron Accepted 19th June 2020 affinity of the central cation, X+. Providing an improved understanding of the fundamental factors DOI: 10.1039/d0sc02076a Creative Commons Attribution 3.0 Unported Licence. determining bond symmetry on a comprehensive level is expected to facilitate future developments and rsc.li/chemical-science applications of secondary bonding and hypervalent chemistry. -
A Textbook Chapter on Solubility Characteristics and the Precipitation of Asphaltenes
The Chemistry of Alberta Oil Sands, Bitumens and Heavy Oils Otto P. Strausz Elizabeth M. Lown Department of Chemistry Department of Chemistry University of Alberta University of Alberta The Alberta Energy Research Institute and Her Majes.ty the Queen in right of Alberta make no warranty, express or implied-, nor assume any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, contained in this publication, nor that use thereof will not infringe on -privately owned ights. The views and opinions of the author expressed herein, do not necessarily reflect 'those of'the Alberta Energy Research Institute or'Her Majesty the Queen in. right of Alberta, The Government of Alberta, its officers, employees, agents, and consultants are exempted, excluded and absolved from all liability for damage or 'injury, howsoever caused, to any person in connection with or arising out of'the use by that person for any purpose -ofthis publication or its contents. Copyright © Dr. Otto Strausz 2003 ISBN 0778530965 Published by: Alberta Energy 'Research 'Institute ~"~'*~'"~ Suite 2540, Monenco Place 801 6th Avenue S.W Calgary Alberta, Canada T2P 3W2 www.aeri.ab.ca Contents Introduction . ............ ....................... ................................... 1 Bibliography.................... .................................... ............. 7 1. The Origin of Petroleum! ............................. ......... 9 1.0 Gen'esis of Petroleum ................................................. 12 2.0 Migration and Accumulation -
2.#Water;#Acid.Base#Reac1ons
8/24/15 BIOCH 755: Biochemistry I Fall 2015 2.#Water;#Acid.base#reac1ons# Jianhan#Chen# Office#Hour:#M#1:30.2:30PM,#Chalmers#034# Email:#[email protected]# Office:#785.2518# 2.1#Physical#Proper1es#of#Water# • Key$Concepts$2.1$ – Water#molecules,#which#are#polar,#can#form#hydrogen#bonds#with# other#molecules.# – In#ice,#water#molecules#are#hydrogen#bonded#in#a#crystalline#array,#but# in#liquid#water,#hydrogen#bonds#rapidly#break#and#re.form#in#irregular# networks.# – The#aTrac1ve#forces#ac1ng#on#biological#molecules#include#ionic# interac1ons,#hydrogen#bonds,#and#van#der#Waals#interac1ons.# – Polar#and#ionic#substances#can#dissolve#in#water.# (c)#Jianhan#Chen# 2# 1 8/24/15 2.1#Physical#Proper1es#of#Water# • Key$Concepts$2.1$ – The#hydrophobic#effect#explains#the#exclusion#of#nonpolar#groups#as#a# way#to#maximize#the#entropy#of#water#molecules.# – Amphiphilic#substances#form#micelles#or#bilayers#that#hide#their# hydrophobic#groups#while#exposing#their#hydrophilic#groups#to#water.# – Molecules#diffuse#across#membranes#which#are#permeable#to#them# from#regions#of#higher#concentra1on#to#regions#of#lower# concentra1on.# – In#dialysis,#solutes#diffuse#across#a#semipermeable#membrane#from# regions#of#higher#concentra1on#to#regions#of#lower#concentra1on.# (c)#Jianhan#Chen# 3# Human#Body#Mass#Composi1on# (c)#Jianhan#Chen# 4 2 8/24/15 Structure#of#Water# (c)#Jianhan#Chen# 5 Water#Hydrogen#Bonding# ~1.8 Å, 180o Acceptor Donor (c)#Jianhan#Chen# 6# 3 8/24/15 Typical#Bond#Energies# (c)#Jianhan#Chen# 7# Hydrogen#bond#networks#of#water/ice# (c)#Jianhan#Chen# -
Intermolecular Forces and Solutions Chapter 7 Forces • Intra-Molecular Forces: Forces Within the Molecule
Intermolecular forces and Solutions Chapter 7 Forces • Intra-molecular forces: Forces within the molecule. Generally stronger. Examples: Ionic, polar covalent and non-polar covalent bonds. • Inter-molecular forces: Generally weaker. Examples: dipole-dipole and hydrogen bonding. • Where do we see the effects of intermolecular forces? • They are the attraction that holds water into its liquid and solid shape. • They are the forces that give water it's surface tension. • They are the forces that break when going from a solid to a liquid or a liquid to a gas. The type of molecule/ion determines the type of intermolecular force. Types of intermolecular forces • Ion-dipole (between ions and polar molecules) • dipole-dipole (between 2 polar molecules) • dipole-induced dipole (between a polar molecule and a non-polar molecules) • induced dipole - induced dipole (between 2 non- polar molecules) Water uses ion-dipole forces to dissolve salts HCl uses Dipole-Dipole Forces Hydrogen Bonding • A particularly strong example of dipole-dipole. • Occurs when there is an OH, NH or FH bond. H is very small and O N and F are very electronegative. Conditions for Hydrogen Bonding • Two important conditions must be met for hydrogen bonding to occur: o One molecule has a hydrogen atom attached by a covalent bond to an atom of N, O, or F. o The other molecule has an N, O, or F atom. Dipole-induced dipole induced dipole - induced dipole (also called London Forces) Larger molecules have more attractions What will be the intermolecular force in a pure substance? Factors that change boiling points • Type of Intermolecular Forces – The stronger the force, the higher the b.p. -
Basic Concepts of Chemical Bonding
Basic Concepts of Chemical Bonding Cover 8.1 to 8.7 EXCEPT 1. Omit Energetics of Ionic Bond Formation Omit Born-Haber Cycle 2. Omit Dipole Moments ELEMENTS & COMPOUNDS • Why do elements react to form compounds ? • What are the forces that hold atoms together in molecules ? and ions in ionic compounds ? Electron configuration predict reactivity Element Electron configurations Mg (12e) 1S 2 2S 2 2P 6 3S 2 Reactive Mg 2+ (10e) [Ne] Stable Cl(17e) 1S 2 2S 2 2P 6 3S 2 3P 5 Reactive Cl - (18e) [Ar] Stable CHEMICAL BONDSBONDS attractive force holding atoms together Single Bond : involves an electron pair e.g. H 2 Double Bond : involves two electron pairs e.g. O 2 Triple Bond : involves three electron pairs e.g. N 2 TYPES OF CHEMICAL BONDSBONDS Ionic Polar Covalent Two Extremes Covalent The Two Extremes IONIC BOND results from the transfer of electrons from a metal to a nonmetal. COVALENT BOND results from the sharing of electrons between the atoms. Usually found between nonmetals. The POLAR COVALENT bond is In-between • the IONIC BOND [ transfer of electrons ] and • the COVALENT BOND [ shared electrons] The pair of electrons in a polar covalent bond are not shared equally . DISCRIPTION OF ELECTRONS 1. How Many Electrons ? 2. Electron Configuration 3. Orbital Diagram 4. Quantum Numbers 5. LEWISLEWIS SYMBOLSSYMBOLS LEWISLEWIS SYMBOLSSYMBOLS 1. Electrons are represented as DOTS 2. Only VALENCE electrons are used Atomic Hydrogen is H • Atomic Lithium is Li • Atomic Sodium is Na • All of Group 1 has only one dot The Octet Rule Atoms gain, lose, or share electrons until they are surrounded by 8 valence electrons (s2 p6 ) All noble gases [EXCEPT HE] have s2 p6 configuration. -
คม 331 เคมีอนินทรีย์1 ปีการศึกษา 1-2561
Chemical Bondings คม 331 เคมีอนินทรีย์ 1 ปีการศึกษา 1-2561 1. บทน า พันธะเคมี (Chemical Bondings) • พันธะเคมี → แรงดึงดูดระหว่างอะตอม โมเลกุล หรือไอออน ท าให้มีความเสถียรเพิ่มขึ้นกว่าเมื่อ อยู่เป็นอะตอม โมเลกุล หรือไอออนเดี่ยวๆ - หัวข้อ • พันธะเคมีเกิดจากการใช้อิเล็กตรอนวงนอก (valence e ) ได้แก่ (1) การให้-รับ valence e- หรือ (2) การใช้ valence e- ร่วมกันระหว่างคู่ที่เกิดพันธะ 1. บทน า 5. เรโซแนนซ์ • พันธะระหว่างอะตอมหรือไอออน มีความแข็งแรงมากกว่าพันธะระหว่างโมเลกุล 2. ประเภทของพันธะเคมี 6. ประจุฟอร์มอล • พันธะเคมี เป็นแรงดึงดูดที่แข็งแรงกว่าแรงทางเคมี 3. แรงระหว่างโมเลกุล 7. กฎ 18 อิเล็กตรอน • พันธะเคมีระหว่างอะตอมหรือไอออน ได้แก่ พันธะไอออนิก พันธะโควาเลนต์ และพันธะโลหะ 4. ทฤษฎีพันธะเคมี 8. พันธะ 3 อะตอม 2 อิเล็กตรอน → เกี่ยวข้องกับสมบัติทางเคมีหรือปฏิกิริยาเคมีของธาตุหรือสารประกอบ • พันธะระหว่างโมเลกุล ได้แก่ พันธะไฮโดรเจนและแรงแวนเดอร์วาลส์ → เกี่ยวข้องกับสมบัติ ทางกายภาพของสารมากกว่าสมบัติทางเคมี เนื้อหาบรรยาย รายวิชา คม 331 เคมีอนินทรีย์ 1 เนื้อหาบรรยาย รายวิชา คม 331 เคมีอนินทรีย์ 1 http://www.chemistry.mju.ac.th/wtms_documentAdminPage.aspx?bID=4093 อ.ดร.เพชรลดา กันทาดี อ.ดร.เพชรลดา กันทาดี 2 พันธะเคมี อาจารย์ ดร.เพชรลดา กันทาดี 1 Chemical Bondings Chemical Bondings 1. บทน า 2. ประเภทของพันธะเคมี • พันธะเคมีระหว่างอะตอม → ระยะระหว่างสองอะตอมจะต้องไม่ไกลเกินไปจนนิวเคลียสของ 1. พันธะไอออนิก (Ionic bond) สองอะตอมไม่ดึงดูดกัน และไม่ใกล้เกินไปจนเกิดแรงผลักระหว่างอิเล็กตรอนของสองนิวเคลียส - บางครั้งเรียกว่า พันธะอิเล็กโทรเวเลนซ์ (electrovalence bond) หรือพันธะ → ระยะที่เหมาะสมนี้ เรียกว่า ความยาวพันธะ ไฟฟ้าสถิตย์ (electrostatic bond) -
Competition of Van Der Waals and Chemical Forces on Gold–Sulfur Surfaces and Nanoparticles
Downloaded from orbit.dtu.dk on: Oct 01, 2021 Competition of van der Waals and chemical forces on gold–sulfur surfaces and nanoparticles Reimers, Jeffrey R.; Ford, Michael J.; Marcuccio, Sebastian M.; Ulstrup, Jens; Hush, Noel S. Published in: Nature Reviews. Chemistry Link to article, DOI: 10.1038/s41570-0017 Publication date: 2017 Document Version Peer reviewed version Link back to DTU Orbit Citation (APA): Reimers, J. R., Ford, M. J., Marcuccio, S. M., Ulstrup, J., & Hush, N. S. (2017). Competition of van der Waals and chemical forces on gold–sulfur surfaces and nanoparticles. Nature Reviews. Chemistry, 1(2), [0017]. https://doi.org/10.1038/s41570-0017 General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. Users may download and print one copy of any publication from the public portal for the purpose of private study or research. You may not further distribute the material or use it for any profit-making activity or commercial gain You may freely distribute the URL identifying the publication in the public portal If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. REVIEW ARTICLE: Competition of van der Waals and chemical forces on gold-sulfur surfaces and nanoparticles Jeffrey R. Reimers1,2, Michael J. Ford2, Sebastian M. Marcuccio3,4, Jens Ulstrup5, and Noel S. -
A New Way for Probing Bond Strength J
A New Way for Probing Bond Strength J. Klein, H. Khartabil, J.C. Boisson, J. Contreras-Garcia, Jean-Philip Piquemal, E. Henon To cite this version: J. Klein, H. Khartabil, J.C. Boisson, J. Contreras-Garcia, Jean-Philip Piquemal, et al.. A New Way for Probing Bond Strength. Journal of Physical Chemistry A, American Chemical Society, 2020, 124 (9), pp.1850-1860. 10.1021/acs.jpca.9b09845. hal-02377737 HAL Id: hal-02377737 https://hal.archives-ouvertes.fr/hal-02377737 Submitted on 27 Mar 2021 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. A New Way for Probing Bond Strength Johanna Klein,y Hassan Khartabil,y Jean-Charles Boisson,z Julia Contreras-Garc´ıa,{ Jean-Philip Piquemal,{ and Eric H´enon∗,y yInstitut de Chimie Mol´eculaire de Reims UMR CNRS 7312, Universit´ede Reims Champagne-Ardenne, Moulin de la Housse 51687 Reims Cedex 02 BP39 (France) zCReSTIC EA 3804, Universit´ede Reims Champagne-Ardenne, Moulin de la Housse 51687 Reims Cedex 02 BP39 (France) {Sorbonne Universit´es,UPMC, Laboratoire de Chimie Th´eoriqueand UMR CNRS 7616, 4 Pl Jussieu, 75252 Paris Cedex 05(France) E-mail: [email protected] Phone: +33(3)26918497 1 Abstract The covalent chemical bond is intimately linked to electron sharing between atoms. -
Starter for Ten 3
Learn Chemistry Starter for Ten 3. Bonding Developed by Dr Kristy Turner, RSC School Teacher Fellow 2011-2012 at the University of Manchester, and Dr Catherine Smith, RSC School Teacher Fellow 2011-2012 at the University of Leicester This resource was produced as part of the National HE STEM Programme www.rsc.org/learn-chemistry Registered Charity Number 207890 3. BONDING 3.1. The nature of chemical bonds 3.1.1. Covalent dot and cross 3.1.2. Ionic dot and cross 3.1.3. Which type of chemical bond 3.1.4. Bonding summary 3.2. Covalent bonding 3.2.1. Co-ordinate bonding 3.2.2. Electronegativity and polarity 3.2.3. Intermolecular forces 3.2.4. Shapes of molecules 3.3. Properties and bonding Bonding answers 3.1.1. Covalent dot and cross Draw dot and cross diagrams to illustrate the bonding in the following covalent compounds. If you wish you need only draw the outer shell electrons; (2 marks for each correct diagram) 1. Water, H2O 2. Carbon dioxide, CO2 3. Ethyne, C2H2 4. Phosphoryl chloride, POCl3 5. Sulfuric acid, H2SO4 Bonding 3.1.1. 3.1.2. Ionic dot and cross Draw dot and cross diagrams to illustrate the bonding in the following ionic compounds. (2 marks for each correct diagram) 1. Lithium fluoride, LiF 2. Magnesium chloride, MgCl2 3. Magnesium oxide, MgO 4. Lithium hydroxide, LiOH 5. Sodium cyanide, NaCN Bonding 3.1.2. 3.1.3. Which type of chemical bond There are three types of strong chemical bonds; ionic, covalent and metallic.