Infrared spectroscopy involves measuring the absorption or emission of electromagnetic radiation by molecules as they undergo transitions between different energy states. Infrared spectroscopy analyzes the infrared region of the electromagnetic spectrum, where molecules absorb radiation based on the vibrational and rotational motions of their bonds. The positions and intensities of absorption bands in an infrared spectrum provide information about the types of bonds in a molecule and can be used to determine its structure.
A ppt compiled by Yaseen Aziz Wani pursuing M.Sc Chemistry at University of Kashmir, J&K, India and Naveed Bashir Dar, a student of electrical engg. at NIT Srinagar.
Warm regards to Munnazir Bashir also for providing us with refreshing tea while we were compiling ppt.
A ppt compiled by Yaseen Aziz Wani pursuing M.Sc Chemistry at University of Kashmir, J&K, India and Naveed Bashir Dar, a student of electrical engg. at NIT Srinagar.
Warm regards to Munnazir Bashir also for providing us with refreshing tea while we were compiling ppt.
PTC IS THE PHASE TRANSFER CATALYSIS HERE TYPES OF PTC ARE DISCUSSED , THEORIES OF CATALYSIS AND MECHANISM OF PTC, ADVANTAGES OF PTC, APPLICATION OF PTC
MASS SPECTROSCOPY ( Molecular ion, Base peak, Isotopic abundance, Metastable ...Sachin Kale
CONTENT:
Molecular Ion Peak
Significance of Molecular ion & Graphically Method
Base Peak
Isotopic Abundance
Metastable Ion
Significance of Metastable ion
Nitrogen Rule & graphs
Formulation of Rule
TRANSITION METAL CATALYSIS , THE DIFFERENT METALS OF TRANSITION USED AS CATALYTIC REAGENT WITH ITS PROPERTIES , THEIR CHARGE TRANSFER ITS REACTION INCLUDING COPPER, PALLADIUM FOLLWED BY HECKMAN, ULLMAN COUPLING REACTION, GILLMAN REACTION, HECK REACTION
Optical activity in catenanes and rotaxanesPRUTHVIRAJ K
These class of compounds do not contain any formal chiral centre but exhibit stereoisomerism due to presence of either a chiral axis or a chiral plane and are called stereoaxis and stereoplanes respectively
Infrared spectroscopy deals with the infrared region of the electromagnetic spectrum, that is light with a longer wavelength and lower frequency than visible light. Infrared Spectroscopy is an analysis of infrared light interacting with a molecule.
The IR spectroscopy can be analyzed in three ways: by measuring absorption, emission, and reflection. The major use of this technique is in organic and inorganic chemistry to determine functional groups of molecules. A basic IR spectrum is essentially a graph of infrared light absorbed on the vertical axis vs. frequency or wavelength on the horizontal axis.
PTC IS THE PHASE TRANSFER CATALYSIS HERE TYPES OF PTC ARE DISCUSSED , THEORIES OF CATALYSIS AND MECHANISM OF PTC, ADVANTAGES OF PTC, APPLICATION OF PTC
MASS SPECTROSCOPY ( Molecular ion, Base peak, Isotopic abundance, Metastable ...Sachin Kale
CONTENT:
Molecular Ion Peak
Significance of Molecular ion & Graphically Method
Base Peak
Isotopic Abundance
Metastable Ion
Significance of Metastable ion
Nitrogen Rule & graphs
Formulation of Rule
TRANSITION METAL CATALYSIS , THE DIFFERENT METALS OF TRANSITION USED AS CATALYTIC REAGENT WITH ITS PROPERTIES , THEIR CHARGE TRANSFER ITS REACTION INCLUDING COPPER, PALLADIUM FOLLWED BY HECKMAN, ULLMAN COUPLING REACTION, GILLMAN REACTION, HECK REACTION
Optical activity in catenanes and rotaxanesPRUTHVIRAJ K
These class of compounds do not contain any formal chiral centre but exhibit stereoisomerism due to presence of either a chiral axis or a chiral plane and are called stereoaxis and stereoplanes respectively
Infrared spectroscopy deals with the infrared region of the electromagnetic spectrum, that is light with a longer wavelength and lower frequency than visible light. Infrared Spectroscopy is an analysis of infrared light interacting with a molecule.
The IR spectroscopy can be analyzed in three ways: by measuring absorption, emission, and reflection. The major use of this technique is in organic and inorganic chemistry to determine functional groups of molecules. A basic IR spectrum is essentially a graph of infrared light absorbed on the vertical axis vs. frequency or wavelength on the horizontal axis.
La región del infrarrojo (IR) del espectro abarca la radiación con números de ondas comprendidos entre 12.800 y los 10 cm-1, que corresponde a longitudes de onda de 0,78, 1.000 μm. Tanto desde el punto de vista de las aplicaciones como de la instrumentación, es conveniente dividir el espectro IR en tres regiones denominadas infrarrojo cercano, medio y lejano. Las técnicas de las aplicaciones de los métodos basados en cada una de estas regiones difieren considerablemente.
Electromagnetic radiation consists of waves of the electromagnetic field, propagating through space, carrying electromagnetic radiant energy. It includes radio waves, microwaves, infrared, light, ultraviolet, X-rays, and gamma rays. All of these waves form part of the electromagnetic spectrum.EMR is released when excited atoms or molecules return to ground state and this process is called emisssion.
EMR has both electric (E) and magnetic (H) components that propagate at right angles to each other.
Infrared spectroscopy is technique to identify the functional group of the molecule.
In Infrared spectroscopy there are two main region finger print region and functional group region. Most of the molecules identifies In the finger print region due to that it is complex region.
Now we will see the
principle of IR spectroscopy:
IR spectroscopy is vibrational energy level changes when IR radiation passes through the material.
Introduction to Spectroscopy,
Introduction to UV, electronic transitions, terminology, chromophore, Auxochrome, Examples and Applications.
Introduction to IR, Fundamental vibrations, Types of Vibrations, Factors affecting the vibrational freaquencies, Group frequencies, examples and applications.
Ultraviolet spetroscopy by Dr. Monika Singh part-1 as per PCI syllabusMonika Singh
UV Visible spectroscopy as per PCI syllabus: Electronic transitions, chromophores, auxochromes, spectral shifts, solvent effect on absorption spectra, Beer and Lambert’s law, Derivation and deviations.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
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- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Why invest into infodemic management in health emergenciesTina Purnat
A lecture discussing the challenge of health misinformation and information ecosystem in public health, how this impacts demand promotion in health, and how this then relates to responding to misinformation and infodemics in health emergencies. Appended with lots of tools, guidance and resources for people who want to do more reading.
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Mastering Wealth: A Path to Financial FreedomFatimaMary4
### Understanding Wealth: A Comprehensive Guide
Wealth is a multifaceted concept that extends beyond mere financial assets. It encompasses a range of elements including money, investments, property, and other valuable resources. However, true wealth also includes non-material aspects such as health, relationships, and personal fulfillment. This guide delves into the various dimensions of wealth, exploring how it can be created, sustained, and enjoyed.
#### Defining Wealth
Traditionally, wealth is defined as the abundance of valuable resources or material possessions. It includes financial assets like cash, savings, stocks, bonds, and real estate. However, a broader understanding of wealth considers factors such as personal well-being, emotional health, social connections, and intellectual growth. This holistic view recognizes that true wealth is not solely about accumulating money but also about enhancing one's quality of life.
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Financial wealth remains a critical component of overall wealth. It provides security, freedom, and the ability to pursue opportunities. Key elements of financial wealth include:
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#### Creating Wealth
Creating wealth involves generating and accumulating financial and non-financial resources. The process can be broken down into several key strategies:
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5. Real Estate: Investing in property can provide rental income and capital appreciation. Real estate is a tangible asset that can hedge against inflation
Non-Invasive assessment of arterial stiffness in advanced heart failure patie...
Infrared presentation
1. Infrared Spectroscopy Spectroscopy is the measurement of the absorption or emission of energy by matter (atoms or molecules) when it is subjected to electromagnetic radiation. A spectrophotometer measures the energy changes that take place within a molecule when it is irradiated and records these changes as spectra . In absorption spectroscopy , molecules absorb energy and undergo transitions from the ground state to an excited state of the molecule. The type of spectroscopy involved will depend on the region of the electromagnetic spectrum that is used as a radiation source. In Infrared Spectroscopy , molecules absorb infrared radiation which brings about changes in stretching and bending motions of the molecule. The radiation absorbed is in the energy range with wavelengths (λ) between 2.5 and 17 μm (4000 cm -1 to 600 cm -1 ). In Electronic (UV-visible) Spectroscopy, molecules absorb radiation in the UV-visible region (200 - 800 nm). This brings about electronic transitions within the molecule. Since absorption of radiation is quantized ( i.e. it is subject to certain quantum mechanical restrictions), only the allowed frequencies of radiation appear as absorption bands in the spectrum.
2. Vibrational Spectroscopy All chemical bonds have a natural frequency of vibration (C-H, O-H, C=O, C-C, C=C) but the exact frequency will depend on their environment, i.e. on the actual structure of the molecule involved. Identification of the vibrational frequencies indicates the different bonds present in a molecule and provides structural information about that molecule. An infrared spectrum is a plot of % transmittance (y-axis) versus energy (cm -1 ) (x-axis) in the range 4000 cm -1 to 600 cm -1 .
3.
4. The Units: The frequency (s -1 ) => # vibrations per second For molecular vibrations, this number is very large (10 13 s -1 ) => inconvenient e.g. = 3 * 10 13 s -1 = 1000 cm -1 Wave Length : 1 = More convenient : Wavenumber = c ( Frequency / Velocity ) = s 3 * 10 10 cm s -1
5. Intensity in IR Intensity: Transmittance ( T ) or %T Absorbance ( A ) IR : Plot of %IR that passes through a sample ( transmittance ) vs Wavelenght T = I I 0 A = log I I 0
9. Introduction IR is one of the first technique inorganic chemists used (since 1940) Molecular Vibration Newton’s law of motion is used classically to calculate force constant r r e F F The basic picture : atoms (mass) are connected with bonding electrons. R e is the equilibrium distance and F : force to restore equilibrium F(x) = - k x where X is displacement from equilibrium Where K i is the force constant and i is reduce mass of a particular motion Because the energy is quantized: E = h i = 1 2 √ k i i
10. Introduction Displacement of atoms during vibration lead to distortion of electrival charge distribution of the molecule which can be resolve in dipole, quadrupole, octopole …. In various directions => Molecular vibration lead to oscillation of electric charge governed by vibration frequencies of the system Oscillating molecular dipole can interact directly with oscillating electric vector of electromagnetic radiation of the same frequency h = h Vibrations are in the range 10 11 to 10 13 Hz => 30 - 3,000 cm -1
11.
12. Calculating stretching frequencies Hooke’s law : : Frequency in cm -1 c : Velocity of light => 3 * 10 10 cm/s K : Force constant => dynes /cm masses of atoms in grams C —C K = 5* 10 5 dynes/cm C =C K = 10* 10 5 dynes/cm C C K = 15* 10 5 dynes/cm = 1 2 c K m 1 m 2 m 1 + m 2 M 1 M 2 M 1 + M 2 (6.02 * 10 23 ) = 4.12 K
13. Calculating stretching frequencies C =C K = 10* 10 5 dynes/cm C —H K = 5* 10 5 dynes/cm C —D K = 5* 10 5 dynes/cm = 4.12 K M 1 M 2 M 1 + M 2 (12)(12) 12 + 12 = 4.12 10* 10 5 = 1682 cm -1 Experimental 1650 cm -1 = 4.12 5* 10 5 = 3032 cm -1 M 1 M 2 M 1 + M 2 (12)(1) 12 + 1 Experimental 3000 cm -1 = 4.12 5* 10 5 = 2228 cm -1 M 1 M 2 M 1 + M 2 (12)(2) 12 + 2 Experimental 2206 cm -1
18. Analyzing an IR spectrum In practice, there are similarities between frequencies of molecules containing similar groups. Group - frequency correlations have been extensively developed for organic compounds and some have also been developed for inorganics
19. Some characteristic infrared absorption frequencies BOND COMPOUND TYPE FREQUENCY RANGE, cm -1 C-H alkanes 2850-2960 and 1350-1470 alkenes 3020-3080 (m) and RCH=CH2 910-920 and 990-1000 R2C=CH2 880-900 cis -RCH=CHR 675-730 (v) trans -RCH=CHR 965-975 aromatic rings 3000-3100 (m) and monosubst. 690-710 and 730-770 ortho -disubst. 735-770 meta -disubst. 690-710 and 750-810 (m) para -disubst. 810-840 (m) alkynes 3300 O-H alcohols or phenols 3200-3640 (b) C=C alkenes 1640-1680 (v) aromatic rings 1500 and 1600 (v) C≡C alkynes 2100-2260 (v) C-O primary alcohols 1050 (b) secondary alcohols 1100 (b) tertiary alcohols 1150 (b) phenols 1230 (b) alkyl ethers 1060-1150 aryl ethers 1200-1275(b) and 1020-1075 (m) all abs. strong unless marked: m, moderate; v, variable; b, broad
20.
21. n -pentane CH 3 CH 2 CH 2 CH 2 CH 3 3000 cm -1 1470 &1375 cm -1 2850-2960 cm -1 sat’d C-H n -pentane CH 3 CH 2 CH 2 CH 2 CH 3 3000 cm -1 1470 &1375 cm -1 2850-2960 cm -1 sat’d C-H
38. Symmetrical and asymmetrical stretch Methyl 2872 cm -1 Symmetrical Stretch Asymmetrical Stretch Anhydride 1760 cm -1 2962 cm -1 1800 cm -1 Amino Nitro 3300 cm -1 3400 cm -1 1350 cm -1 1550 cm -1 — C — H H H — C — H H H O O O O O O — N H H — N H H — N O O — N O O
39. General IR comments Precise treatment of vibrations in molecule is not feasible here Some information from IR is also contained in MS and NMR Certain bands occur in narrow regions : OH , CH , C=O Detail of the structure is revealed by the exact position of the band e.g. Ketones 1715 cm -1 1680 cm -1 Region 4000 – 1300 : Functional group Absence of band in this region can be used to deduce absence of groups Caution: some bands can be very broad because of hydrogen bonding e.g. Enols v.broad OH, C=O absent!! Weak bands in high frequency are extremely useful : S-H, C C, C N Lack of strong bands in 900-650 means no aromatic
40. Alkanes , Alkenes , Alkynes C-H : <3000 cm -1 >3000 cm -1 3300 cm -1 sharp C-C Stretch Not useful C=C C C 1660-1600 cm -1 conj. Moves to lower values Symmetrical : no band 2150 cm -1 conj. Moves to lower values Weak but very useful Symmetrical no band Bending CH 2 Rocking 720 cm -1 indicate Presence of 4-CH 2 1000-700 cm -1 Indicate substitution pattern C-H ~630 cm -1 Strong and broad Confirm triple bond
43. Alkene : 1-Decene To give rise to absorption of IR => Oscillating Electric Dipole Symmetry Molecules with Center of symmetry Symmetric vibration => inactive Antisymmetric vibration => active
44. Alkene In large molecule local symmetry produce weak or absent vibration C=C R R trans C=C isomer -> weak in IR Observable in Raman
45. Alkene: Factors influencing vibration frequency 1- Strain move peak to right (decrease ) angle 1650 1646 1611 1566 1656 : exception 2- Substitution increase 3- conjugation decrease C=C-Ph 1625 cm -1 1566 1641 1675 1611 1650 1679 1646 1675 1681 C C C
49. In IR, Most important transition involve : Ground State ( i = 0) to First Excited State ( i = 1) Transition ( i = 0) to ( J = 2) => Overtone
50. IR : Aromatic =C-H > 3000 cm -1 C=C 1600 and 1475 cm -1 =C-H out of plane bending: great utility to assign ring substitution overtone 2000-1667: useful to assign ring substitution e.g. Naphthalene: Substitution pattern Isolated H 862-835 835-805 760-735 2 adjacent H 4 adjacent H out of plane bending
55. IR: Alcohols and Phenols O-H Free : Sharp 3650-3600 O-H H-Bond : Broad 3400-3300 Intermolecular Hydrogen bonding Increases with concentration => Less “Free” OH
56. IR: Alcohols and Phenols C-O : 1260-1000 cm -1 (coupled to C-C => C-C-O) C-O Vibration is sensitive to substitution: Phenol 1220 3` Alcohols 1150 2` Alcohols 1100 1` Alcohols 1050 More complicated than above: shift to lower Wavenumber With unsaturation (Table 3.2)
63. IR: Carbonyl From 1850 – 1650 cm -1 Ketone 1715 cm -1 is used as reference point for comparisons 1715 1690 1725 1700 1710 1680 1810 Anhydr Band 1800 Acid Chloride 1760 Anhydr Band 2 1735 Ester 1725 Aldehyde 1715 Ketone 1710 Acid 1690 Amide Factor influencing C=O 1) conjugation Conjugation increase single bond character of C=O Lower force constant lower frequency number C=C C O C + — C C O -
65. Ketone and Ring Strain Ring Strain: Higher Factors influencing C=O 2) Ring size 1715 cm -1 Angle ~ 120 o 1751 cm -1 < 120 o 1775 cm -1 << 120 o
66.
67. Factors influencing carbonyl: C=O 3) substitution effect (Chlorine or other halogens) Result in stronger bound higher frequency 1750 cm -1 4) Hydrogen bonding Decrease C=O strenght lower frequency 1680 cm -1 — C — C — X O
76. Carbonyl compounds : Acids Carboxylic acid Exist as dimer : Strong Hydrogen bond OH : Very broad 3400 – 2400 cm -1 C=O : broad 1730 – 1700 cm -1 C — O : 1320 – 1210 cm -1 Medium intensity
77. Carbonyl compounds : Acids C=O OH C=O : 1711 cm -1 OH : Very Broad 3300 to 2500 cm -1 C-O : 1285, 1207 cm -1
78. Anhydrides C=O always has 2 bands: 1830-1800 and 1775-1740 cm -1 C —O multiple bands 1300 – 900 cm -1
79. Carbonyl compounds : Aldehydes Aldehydes C=O ~ 1725 cm -1 O=C-H : 2 weak bands 2750, 2850 cm -1 Conjugation => lower freq. C=O : 1724 cm -1
82. Other carbonyl Amides Lactams Acid Chlorides C=O ~1680-1630 cm -1 (band I) NH 2 ~ 3350 and 3180 cm -1 (stretch) NH ~ 3300 cm -1 (stretch) NH ~ 1640-1550 cm -1 (bending) 1810-1775 cm -1 C — Cl 730 – 550 cm -1 ~1660 ~1705 ~1745 Increase with strain R — C — Cl O
83. Amides NH 2 : Symmetrical stretch =>3170 cm -1 asymmetrical stretch => 3352 cm -1 C=O : 1640 cm -1 NH Out of plane
91. Other Nitrogen Compounds Nitriles Isocyanates Isothiocyanates Imines / Oximes R-C N : Sharp 2250 cm -1 Conjugation moves to lower frequency R-N=C=O Broad ~ 2270 cm -1 R-N=C=S 2 Broad peaks ~ 2125 cm -1 R 2 C=N-R 1690 - 1640 cm -1
95. Nitro Aliphatic : Asymmetric : 1600-1530 cm -1 Symmetric : 1390-1300 cm -1 Aromatic : Asymmetric : 1550-1490 cm -1 Symmetric : 1355-1315 cm -1 — N O O + -
98. Sulfur Mercaptans S – H : weak 2600-2550 cm -1 Since only few absorption in that range it confirm its presence Sulfides,Disulfides : no useful information Sulfoxides: Strong ~ 1050 cm -1 Sulfones : Asymetrical ~ 1300 cm -1 Symetrical ~ 1150 cm -1 2 bands :
101. Sulfur: Sulfonate S=O : Asymmetrical stretch: 1350 cm-1 Symmetrical Stretch : 1175 cm-1 S-O : several bands between 1000 – 750 cm -1
102. Sulfur: Sulfonamide S=O : Asymmetrical stretch: 1325 cm-1 Symmetrical Stretch : 1140 cm-1 NH 2 stretch: 3350 and 3250 cm -1 NH Bend: 1550 cm -1
103. Halogens C —F : 1400 – 1000 cm -1 C —Cl : strong 785 – 540 cm -1 C —Br : 650 – 510 cm -1 (out of range with NaCl plates) C —I : 600 – 485 cm -1 (out of range)
105. Phosphorus Phosphines: R-PH 2 R 2 PH P —H : Sharp 2320 – 2270 cm -1 P H 2 bending : 1090 – 1075 and 840 - 810 cm -1 P H bending : 990 - 886 cm -1 Phosphine Oxide : R 3 P=O P =O very strong : 1210 - 1140 cm -1 Phosphate Esters : (OR) 3 P=O P =O very strong : 1300 - 1240 cm -1 P -O very strong : 1088 – 920 cm -1 P -O : 845 - 725 cm -1
106. Silicon IR-Organometallic Index Si-H : 2200 cm -1 (Stretch) 950 – 800 cm -1 (bend) Si-O-H : OH: 3700 – 3200 cm -1 (Stretch) Si-O : 830 – 1110 cm -1