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10.1.13 FORCES GOVERNING BIOLOGICAL SYSTEMS
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Electronic structure of atoms Negatively charged electrons revolve around positively charged nucleus. Atom is neutral Shells: The electrons move around the atomic nuclei in discrete, concentric volumes, the shells. The electrons of each shell possess a definite energy with reference energy numbers n = 1, 2, 3 ….. designated K, L, M, N …….. The maximum number of electrons which each shell accommodates is 2n 2..Due to Coulomb interaction between electrons and nucleus the electrons tend to occupy the shells as close to the nucleus as possible
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Orbitals: Angular momentum quantum number Orbitals: Electrons behave both as particles and as waves. It is not possible to accurately determine the position of the electron because of its wave nature. The regions within each shell in which the electrons are most likely to be found are known as orbital Based on the shape of the orbital and the angular momentum electrons exhibit when located within the orbital, an angular momentum quantum number l is assigned
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Orbitals ‘l’ can have values l=0, 1…..n-1 designated as s, p, d, f… s-orbital is spherical in shape, d-orbital is dumbbell shaped with constriction in the region of the nucleus, d-orbital is double dumbbell shaped
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Orientations of Orbitals Another quantum number called “magnetic quantum number, m” is assigned to electrons depending on the orientation of orbital in space m can have values from –l,…..-1,0,1…..+l For l=0, m=0. s-orbital can have only one orientation. So there is only one s-orbital per shell For l=1, m=-1,0,1. p-orbital can have three orientations designated as p x, p y, p z d-orbitals (l=2) can have five orientations so there are five d-orbitals per shell. Similarly a shell can have seven f-orbitals
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Electron Spin A fourth quantum number “s” denotes the spin of electron. ‘s’ can have +1/2 value (spin up ) or -1/2 (spin down ) According to Pauli’s exclusion principle “No two electrons of a given atom are allowed to possess the same four quantum numbers at a time” Each orbital can therefore have a maximum of two electrons one with spin up and other with spin down
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When there are many orbitals, orbitals of each type are first filled singly. Only after all these orbitals contain one electron each, a second electron is added to the orbitals to complete a pair and thereby fill the orbital The elements that life is primarily made up of are: Hydrogen (H), Carbon (C), nitrogen (N), oxygen (O) and phosphorus (P) H: 1s 1 C: 1s 2, 2s 2, 2p 2 O: 1s 2,2s 2,2p 4 N: 1s 2, 2s 2, 2p 3 P: 1s 2, 2s 2, 2p 6,3s 2,3p 3
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Intramolecular and intermolecular forces Intramolecular Forces Ionic bonds which is the attraction between positive and negative ions in a crystal of an ionic compound Covalent bonds Metallic bonds Intermolecular Forces Hydrogen bonding Van der Waals forces
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Ionic bond An electropositive atom loses an electron forming a cation. This electron is gained by an electronegative atom forming an anion. These ions being oppositely charged will be attracted towards each other by Coulombic attraction e.g. NaCl Na Na + + 1e - Cl + 1e - Cl -
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Covalent bonds Bond formed when atoms achieve the octet configuration by sharing their electrons. The orbitals of atoms sharing their electrons overlap and their electrons move into a new orbital called “Molecular orbital” where the pair of electrons are attracted towards both the nuclei
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Polar & Nonpolar Covalent Bonds Non polar covalent bond: with equal sharing of the bond electrons, arise when the electronegativities of the two atoms are equal. Polar covalent bond A bond between 2 atoms that have different electronegativities and therefore have unequal sharing of the bonding electron pair
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Coordinate covalent bond A coordinate covalent bond is a covalent bond in which both electrons are furnished by one atom These bonds involve unequal sharing of electron pair by two atoms. The electron pair donor is the ligand or Lewis base while the acceptor is Lewis acid These bonds are formed between transition metals (central atoms) and organic ligands e.g. Fe 2+ in hemoglobin and the cytochromes
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Coordinate Covalent Bonds in Hemoglobin Hemoglobin is a very large molecule (a macromolecule), but of all the atoms in this molecule, the only ones that concern us here are four iron atoms. Each of these four atoms is embedded in a portion of the hemoglobin called heme. An iron atom in the center is held in place by covalent bonds to two nitrogen atoms and by coordinate covalent bonds to two other nitrogen atoms.
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The protein called hemoglobin carry oxygen, O 2 to the cells of the body. The O 2 attaches itself to the hemoglobin by a coordinate covalent bond When hemoglobin picks up oxygen in the lungs, each O 2 molecule bonds to one of the Fe atoms by a coordinate covalent bond, with both electrons supplied by the oxygen, because the Fe atom, though bonded to four N atoms, still has room for additional electrons Coordinate Covalent Bonds in Hemoglobin
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Carbon monoxide poisoning The coordinate covalent bonding ability of the Fe in hemoglobin is not restricted to O 2. There are many other species that are also able to use an electron pair to form such a bond with the Fe in hemoglobin. Among these is the poison carbon monoxide, CO. Carbon monoxide is poisonous because the bond it forms with the Fe in hemoglobin is stronger than the O 2 -Fe bond. When a person breathes in CO the hemoglobin combines with this molecule rather than with O 2. The cells, deprived of O 2, can no longer function, and the person dies.
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Hydrogen Bonding Hydrogen bonding can be both “intramolecular” as well as “intermolecular” When a hydrogen atom is covalently linked with a strongly electronegative atom such as oxygen or nitrogen, it carries a partial positive charge Hydrogen bonding is the interaction occurring between the partial positively charged H atom of a proton donor group A-H and a region of high electron density (e.g. a lone pair) of a proton acceptor group B (A is an electronegative atom)
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Intramolecular Hydrogen Bonding Intramolecular H-bonding occurs in molecules where the proton donor group and the proton acceptor group belongs to the same molecule Here the proton donor and the proton acceptor sites on the same molecule is in a favorable spatial configuration to form a H-bond
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This positively charged hydrogen atom gets attracted towards the negative end of another molecule and this attraction weakly binds the two molecules A number of molecules attracted to each other by these electrostatic forces may associate together to form large clusters of molecules with hydrogen acting as bridge between the electronegative atoms Intermolecular Hydrogen Bonding Intermolecular hydrogen bonding is the attractive force between covalently bonded hydrogen atom of one molecule with the lone pair of an electronegative atom of another molecule
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H- bonding in Proteins
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Hydrogen Bonding in Nucleic Acids
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Vander Waals Forces (Intermolecular) Ion-dipole interaction Dipole-dipole interaction (Keesom forces) Dipole induced dipole Interaction (Debye forces) Instantaneous dipole-induced dipole forces (London dispersion forces)
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Ion-dipole interaction
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Force between two permanent dipoles (Keesom force) ++ –– ++ –– ++ –– ++ ––
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Force between a permanent dipole and a corresponding induced dipole (Debye force)
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London Forces Non-polar molecules do not have dipoles like polar molecules Though the electron density in an atom or a molecule is constant, there occurs a rapid but continuous oscillation of electrons (fluctuation of electron density) with respect to the nucleus As a result, at a given instant, positive charges may be concentrated at one end & negative charges to another region of molecule. Thus a nonpolar molecule may become momentarily polarized-an instantaneous dipole and this dipole may attract other molecules by a dipole induced dipole mechanism
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London Forces
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Hydrophobic Interactions These interactions cause non-polar side chains (aromatic rings and hydrocarbon groups) to cling together in polar solvents especially water Non-polar groups try to arrange themselves in such a way that they are not in contact with water molecules i.e. water has a tendency to exclude non-polar groups
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