Ala-Arg-Pro-Tyr-Asn-Phe-Cpa-Leu-NH 2

Similar documents
= I, (I - 1), (I - 2),, -I

Laboratory and Rotating frames

Topics. The History of Spin. Spin. The concept of spin Precession of magnetic spin Relaxation

7a. Structure Elucidation: IR and 13 C-NMR Spectroscopies (text , , 12.10)

Polarization transfer

Magnetic Resonance Imaging (MRI)

Magnetic Resonance Spectroscopy EPR and NMR

Chemistry 213 Practical Spectroscopy

nm nm

NMR BMB 173 Lecture 16, February

Chapter 13 Spectroscopy

Final Exam: CHEM/BCMB 4190/6190/8189 (276 pts) Thursday, 15 December, 2005

Fundamental MRI Principles Module 2 N. Nuclear Magnetic Resonance. X-ray. MRI Hydrogen Protons. Page 1. Electrons

V27: RF Spectroscopy

Topics. Spin. The concept of spin Precession of magnetic spin Relaxation Bloch Equation

Chem 325 NMR Intro. The Electromagnetic Spectrum. Physical properties, chemical properties, formulas Shedding real light on molecular structure:

10.4 Continuous Wave NMR Instrumentation

NMR, the vector model and the relaxation

Coherence selection and multiple quantum spectroscopy.

CHEM6416 Theory of Molecular Spectroscopy 2013Jan Spectroscopy frequency dependence of the interaction of light with matter

Fundamental MRI Principles Module Two

DETECTION OF UNPAIRED ELECTRONS

NMR Spectroscopy. for 1 st B.Tech INTRODUCTION Lecture -1 Indian Institute of Technology, Dhanbad

Nuclear Magnetic Resonance (NMR) Spectroscopy Introduction:

Spectroscopy. a laboratory method of analyzing matter using electromagnetic radiation.

10.3 NMR Fundamentals

Spectroscopy. a laboratory method of analyzing matter using electromagnetic radiation

Arrangement of Electrons in Atoms

where, c is the speed of light, ν is the frequency in wave numbers (cm -1 ) and µ is the reduced mass (in amu) of A and B given by the equation: ma

Spectral Broadening Mechanisms

COPYRIGHTED MATERIAL. Production of Net Magnetization. Chapter 1

With that first concept in mind, it is seen that a spinning nucleus creates a magnetic field, like a bar magnet

III Spins and their Thermodynamics

Lecture 5: Bloch equation and detection of magnetic resonance

Lecture 02 Nuclear Magnetic Resonance Spectroscopy Principle and Application in Structure Elucidation

Chapter 7. Nuclear Magnetic Resonance Spectroscopy

Lecture 2 nmr Spectroscopy

Principles of Molecular Spectroscopy: Electromagnetic Radiation and Molecular structure. Nuclear Magnetic Resonance (NMR)

Principles of Molecular Spectroscopy

Nuclear Magnetic Resonance Spectroscopy

NMR Spectroscopy Laboratory Experiment Introduction. 2. Theory

Lecture outline: Chapter 6 Electronic structure of atoms. Electronic structure of atoms

Lecture 19: Building Atoms and Molecules

Infrared Spectroscopy: Identification of Unknown Substances

Spectral Broadening Mechanisms. Broadening mechanisms. Lineshape functions. Spectral lifetime broadening

3.15 Nuclear Magnetic Resonance Spectroscopy, NMR

NMR Nuclear Magnetic Resonance Spectroscopy p. 83. a hydrogen nucleus (a proton) has a charge, spread over the surface

NUCLEAR MAGNETIC RESONANCE. The phenomenon of nuclear magnetic resonance will be used to study magnetic moments of nuclei.

Topics. The concept of spin Precession of magnetic spin Relaxation Bloch Equation. Bioengineering 280A Principles of Biomedical Imaging

Normalization and Zero-Point Energy The amplitude A 2 in Eq can be found from the normalizing equation, 1106 CHAPTER 39 MORE ABOUT MATTER WAVES

Chemistry 431. Lecture 23

MOLECULAR SPECTROSCOPY AND PHOTOCHEMISTRY

Lecture 3 NMR Spectroscopy. January 26, 2016 Chemistry 328N

Nuclear Magnetic Resonance Imaging

ELECTRON SPIN RESONANCE & MAGNETIC RESONANCE TOMOGRAPHY

The rest of topic 11 INTRODUCTION TO ORGANIC SPECTROSCOPY

A Hands on Introduction to NMR Lecture #1 Nuclear Spin and Magnetic Resonance

The NMR Inverse Imaging Problem

( ) x10 8 m. The energy in a mole of 400 nm photons is calculated by: ' & sec( ) ( & % ) 6.022x10 23 photons' E = h! = hc & 6.

Nuclear Magnetic Resonance

NMR Spectroscopy. Guangjin Hou

Slide 1. Slide 2 What s this thing called light? Slide 3 Freeze the wave and walk. Electronic Structure of Atoms. Chemistry is Electrons

1 Magnetism, Curie s Law and the Bloch Equations

Nuclear Magnetic Resonance Spectroscopy

1.6 ELECTRONIC STRUCTURE OF THE HYDROGEN ATOM

Welcome to MR! CT PET (with FDG) MRI (T2 w.) MR Image types: T2 weighted T1 weighted Sequence parameters FLAIR Diffusion

MRI Homework. i. (0.5 pt each) Consider the following arrangements of bar magnets in a strong magnetic field.

3D Schrödinger Eq. Today: Continue with hydrogen. Multi-electron atoms

Ψ t = ih Ψ t t. Time Dependent Wave Equation Quantum Mechanical Description. Hamiltonian Static/Time-dependent. Time-dependent Energy operator

Lecture 19: Building Atoms and Molecules

Electron Spin Resonance, Basic principle of NMR, Application of NMR in the study of Biomolecules, NMR imaging and in vivo NMR spectromicroscopy

Lecture 3: Light absorbance

CHEM Atomic and Molecular Spectroscopy

Biochemistry 530 NMR Theory and Practice

Nuclear magnetic resonance spectroscopy

Spectroscopy and Chromatography

Introduction. The analysis of the outcome of a reaction requires that we know the full structure of the products as well as the reactants

Basic p rinciples COPYRIGHTED MATERIAL. Introduction. Atomic s tructure

Introduction to Nuclear Magnetic Resonance Spectroscopy

Spin. Nuclear Spin Rules

NMR in Medicine and Biology

NPTEL/IITM. Molecular Spectroscopy Lectures 1 & 2. Prof.K. Mangala Sunder Page 1 of 15. Topics. Part I : Introductory concepts Topics

MRI Physics I: Spins, Excitation, Relaxation

Spectroscopy in Organic Chemistry. Types of Spectroscopy in Organic

Magnetic resonance imaging MRI

NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY

Chapter 6 Part 1 Structure of the atom

Ch 7 Quantum Theory of the Atom (light and atomic structure)

Nuclear Magnetic Resonance (NMR)

Optical Spectroscopy 1 1. Absorption spectroscopy (UV/vis)

5.61 Physical Chemistry Lecture #36 Page

Skoog Chapter 6 Introduction to Spectrometric Methods

Introduction of Key Concepts of Nuclear Magnetic Resonance

NMR Quantum Computation

Nuclear Magnetic Resonance Spectroscopy

Chapter 16 Nuclear Magnetic Resonance Spectroscopy

HST.583 Functional Magnetic Resonance Imaging: Data Acquisition and Analysis Fall 2008

Nuclear Magnetic Resonance Spectroscopy

Rotation and vibration of Molecules

3. Write ground-state electron configurations for any atom or ion using only the Periodic Table. (Sections 8.3 & 9.2)

Transcription:

Applied Spectroscop Ala-Arg-Pro-Tr-Asn-Phe-Cpa-Leu-NH 2 Cpa Ala Pro Guillermo Mona

What is Spectroscop? Without going into latin or greek, spectroscop is the stud of the interactions between light and matter. Here light refers to an sort of electromagnetic radiation, such as visible light, UV, IR, and radiowaves. Depending on the frequenc or wavelength of the radiation involved we will have different tpes of interactions with matter (molecules). The following chart shows the ranges (wavelengths), for different tpes of spectroscopies. γ-ras -ras UV VIS IR µ-wave radio 10-10 10-8 10-6 10-4 10-2 10 0 10 2 wavelength (λ, cm) As ou know, wavelength and frequenc are inversel proportional, so higher frequencies mean shorter wavelength.

Some background Also to remember throughout the course is the relationship between energ and frequenc. The two are related b one of the fundamental equations of quantum mechanics: E = h ν Therefore, the higher the frequenc, the higher the energ. In addition, and as said before, depending on the frequenc and wavelength we ll have different interactions with matter (molecules). The following is a brief list of these: E γ-ras/x-ras - inner shell electrons, nucleus UV/Vis - bonding electrons (valence electrons) IR - Bond length/angle/torsion vibrations NMR - Nuclear spin λ

Wh bother learning NMR? Structural (chemical) elucidation Natural product chemistr. Organic chemistr. Analtical tool of choice for snthetic chemists. Stud of dnamic processes Reaction kinetics. Stud of equilibrium (chemical or structural). Structural (three-dimensional) studies Proteins. DNA/RNA. Protein complees with DNA/RNA. Polsaccharides Drug design Structure Activit Relationships (SAR) b NMR Medicine - Magnetic Resonance Imaging (MRI) Finall, it s the biggest, meanest, most epensive piece of equipment ou ll see in our career at USP, and this is a great time to get our hands on it...

The gor details Absorption (or emission) spectroscop, as IR or UV. Detects the absorption of radiofrequencies (electromagnetic radiation) b certain nuclei in a molecule. Unfortunatel, some quantum mechanics are needed to understand it (a lot to reall understand it ). As opposed to the atomic mass or charge, the spin has no macroscopic equivalent. It eists, period... Onl nuclei with spin number (I) 0 can absorb/emit electromagnetic radiation. Even atomic mass & number I = 0 ( 12 C, 16 O) Even atomic mass & odd number I = whole integer ( 14 N, 2 H, 10 B) Odd atomic mass I = half integer ( 1 H, 13 C, 15 N, 31 P) The spin states of the nucleus (m) are quantied: m = I, (I - 1), (I - 2),, -I Properl, m is called the magnetic quantum number.

Background (continued) For 1 H, 13 C, 15 N, 31 P (biologicall relevant nuclei with I = 1 / 2 ): m = 1 / 2, - 1 / 2 This means that onl two states (energ levels) can be taken b these nuclei. Another important parameter of each particular nuclei is the magnetic moment (µ), which can be epressed as: µ = γ I h / 2ππ It is a vector quantit that gives the direction and magnitude (or strength) of the nuclear magnet h is the Planck constant γ is the gromagnetic ratio, and it depends on the nature of each nuclei. Different nuclei have different magnetic moments. The energ of a spin in a magnetic field will depend on the magnetic field, which we call, and µ:

Magnetic energ and populations When the field is applied, spins have to possible energ limits. In one we are in favor of the field, and in the other one we are against it. The energ is the dot product of the corresponding vectors: E = - µ. µ µ E α = - γ h / 4π E β = γ h / 4π The energ difference of the two levels, α and β, is: E = γ h / 2π The bigger, the larger the energ difference. Also, the population ratio between the two levels depends on E, and we can calculate it as a Boltmman distribution. The E for 1 H s at 400 MH ( = 9.4 T) is 4 10-5 Kcal / mol. N α / N β = e E / RT The N α / N β ratio is onl 1.000064. In one million spins we have a difference of just 64: NMR is ver insensitive when compared to UV or IR...

Magnetic energ, sensitivit, and frequenc Nuclei with larger γ will absorb/emmit more energ, and will therefore be more sensitive. Sensitivit is proportional to µ, to N α / N β, and to the magnetic flu of the coil, all of which depend on γ. In sum, sensitivit is proportional to γ 3. γ 13 C = 6,728 rad / G γ 1 H = 26,753 rad / G 1 H is ~ 64 times more sensitive than 13 C onl due to γ. If we also take into account the natural abundance, 13 C (~1%) ends up being 6400 less sensitive than 1 H... Energ is related to frequenc (quantum mechanics...): E = h ν o E = γ h / 2π ν o = γ / 2π For 1 H s in normal magnets (2.35-18.6 T), the frequencies are between 100 and 800 MH. For 13 C, 1/4 of this γ-ras X-ras UV VIS IR µ-wave radio 10-10 10-8 10-6 10-4 10-2 10 0 10 2 wavelenght (cm)

Precession To eplain everthing in NMR we have to refer to rotation, and H are not the best units to do this. We define the precession or Larmor frequenc, ω o, in radians: ω o = 2πν πν o ω o = γ (radians) With what precession is ω o related to? One thing we left out of the mi was the angular momentum, L, asociated will all nuclei (magnetic or not). We can think of nuclei as small magnetied tops that spin on their ais: L µ After turning the magnet on we ll have two forces acting on the spins. One that tries to turn them towards, and the other that wants to maintain their angular momentum. The net result is that the nuclei spins like a top: ω o L µ

Precession (continued) Now we have to go against a concept used b lots of people to eplain NMR: Spins won t align with, no matter what their intiial orientation was. Spins pointing up and down don t eist! Spins will precess at the angle the were when we turned on the magnetic field : There are several magnetic fields acting on the spins. One is, which is constant in time and generates the precession at ω o. The others are fluctuating due to the molecular anisotrop and its environment, and make the spins tr all the possible orientations with respect to in a certain ammount of time. Orientations in favor of will have lower magnetic energ, and will be slightl favored. After a certain time (the longitudinal relaation, more later), a net magnetiacion (M o ) pointing in the direction of will develop.

Net magnetiation Where does the net magnetiation comes from? In order to figure it out we translate all the spins to the origin of the coordinate ssmem. We ll see something like this: We ll have a slight ecess of spins aligned with, but at an angle with respect to. The distribution is proportional to N α / N β. If we decompose the µ vectors in and <>, we get: = M o = 0 The net magnetiation is aligned with, and this is what we use in NMR.

NMR ecitation So far nothing happened. We have a little tube spinning in the magnet. To see something we have to move the sstem awa from equilibrium. That is, we have to perturb its populations. We need the sstem to absorb energ. The energ source is an oscillating electromagnetic radiation generated b an alternating current: B 1 = C * cos (ω o t) M o B 1 i Transmitter coil () How is that something that has a linear variation can be thought as circular field? A linear variation in is the linear combination of two counter-rotating circular fields: -ω o +ω o = +

For part of the period of oscillation: = + = + We go through ero and then it repeats = + Onl the one vector that rotates at +ω o (in the same direction of the precession of M o ) interacts with the bulk magnetiation. -ω o is the one normall used, but it s just a convention...

Now we throw M o on the mi... When the frequenc of the alternating current is ω o, the frequenc of the right vector of B 1 is ω o and we achieve a resonant condition. The alternating magnetic field and all the µ s interact, there s a torque generated, and the rotate. Since the all rotate the same ammount, the macroscopic effect is that M o rotates around the ais (in this case...), and we generate transverse magnetiation (M ): M o B 1 off B 1 (or off-resonance) M ω o ω o Since we altered the population ratio between energ levels (i.e., N / N α β ), the sstem absorbed energ and we altered the equilibrium... Since the individual spins keep precessing under the effect of, the transverse magnetiation M will rotate around the ais at the precession frequenc, ω o.

Detection of M and return to equilibrium In the absence of the eternal B 1, M will tr to go back to the ais (M o, equilibrium) b restoring the original N α / N β. distributiuon. We ll see the phsics that rule this phenomenon (relaation) later. M returns to the ais precessing on the <> plane (to damned hard to draw ): equilibrium... M o M ω o The oscillation of M generates a fluctuating magnetic field which can be used to generate a current in a coil: M ω o Receiver coil () NMR signal