UV spectroscopy is an analytical method used to detct the numbers of double and triple bonds present in dienes ,trienes and polyenes compounds.The energy corresponds to EM radiation in the ultraviolet (UV) region, 100-350 nm, and visible (VIS) regions 350-700 nm of the spectrum is known as UV spectrum.
It is an analytical technique useful for the determination of molecular mass, molecular formula and fragmentation pattern of particular molecule and compounds. It has greater application in pharmaceutical and medicinal fields.
UV/Vis spectroscopy is routinely used in analytical chemistry for the quantitative determination of different analytes, such as transition metal ions, highly conjugated organic compounds, and biological macromolecules. Molecules containing bonding and non-bonding electrons undergo electronic transitions and absorb energy in the form of ultraviolet or visible light to excite these electrons to higher anti-bonding molecular orbitals.
Uv-Vis spectroscopy: electronic spectroscopy, absorption and emission, Terms describing UV absorptions, absorbing species containing s,n and pi, absorbing species,sigma and pi orbitals, electronic transitions, Absorption: physical Basis and lineshape,UV-Spectra.
Electron Spin Resonance (ESR) SpectroscopyHaris Saleem
Electron Spin Resonance Spectroscopy
Also called EPR Spectroscopy
Electron Paramagnetic Resonance Spectroscopy
Non-destructive technique
Applications
Extensively used in transition metal complexes
Deviated geometries in crystals
Describe the Schroedinger wavefunctions and energies of electrons in an atom leading to the 3 quantum numbers. These can be also observed in the line spectra of atoms.
UV spectroscopy is an analytical method used to detct the numbers of double and triple bonds present in dienes ,trienes and polyenes compounds.The energy corresponds to EM radiation in the ultraviolet (UV) region, 100-350 nm, and visible (VIS) regions 350-700 nm of the spectrum is known as UV spectrum.
It is an analytical technique useful for the determination of molecular mass, molecular formula and fragmentation pattern of particular molecule and compounds. It has greater application in pharmaceutical and medicinal fields.
UV/Vis spectroscopy is routinely used in analytical chemistry for the quantitative determination of different analytes, such as transition metal ions, highly conjugated organic compounds, and biological macromolecules. Molecules containing bonding and non-bonding electrons undergo electronic transitions and absorb energy in the form of ultraviolet or visible light to excite these electrons to higher anti-bonding molecular orbitals.
Uv-Vis spectroscopy: electronic spectroscopy, absorption and emission, Terms describing UV absorptions, absorbing species containing s,n and pi, absorbing species,sigma and pi orbitals, electronic transitions, Absorption: physical Basis and lineshape,UV-Spectra.
Electron Spin Resonance (ESR) SpectroscopyHaris Saleem
Electron Spin Resonance Spectroscopy
Also called EPR Spectroscopy
Electron Paramagnetic Resonance Spectroscopy
Non-destructive technique
Applications
Extensively used in transition metal complexes
Deviated geometries in crystals
Describe the Schroedinger wavefunctions and energies of electrons in an atom leading to the 3 quantum numbers. These can be also observed in the line spectra of atoms.
Coordination Compounds - CHARACTERIZATION AND OVERVIEW, DETECTION OF COMPLEX FORMATION, Formation of precipitate, Conductivity measurements , Change in chemical behaviour, Spectral methods, Magnetic Method, Spectral Calculations, Term symbols, Mulliken term symbols, Orgel diagrams - d1 configuration in Oh environment , d9 configuration in Oh environment, d1 configuration in Oh environment, Limitations Tanabe sugano diagrams, d2 configuration in Oh environment , Advantages over Orgel’s, Racah parameters
Simulation Of Algan/Si And Inn/Si Electric - Devicesijrap
In this work, efficient solar-blind metal-semiconductor photodetectors grown on Si (111) by
molecular beam epitaxy are reported. Growth details are described,the comparison enters the
properties electric of InN/Si and AlGaN/Si photodectors with 0.2 µm of AlGaN and InN layers.
Modeling and simulation were performed by using ATLAS-TCAD simulator. Energy band
diagram, doping profile, conduction current density,I-V caracteristic , internal potential and
electric field were performed.
Simulation of AlGaN/Si and InN/Si ELECTRIC –DEVICESijrap
In this work, efficient solar-blind metal-semiconductor photodetectors grown on Si (111) by
molecular beam epitaxy are reported. Growth details are described,the comparison enters the
properties electric of InN/Si and AlGaN/Si photodectors with 0.2 μm of AlGaN and InN layers.
Modeling and simulation were performed by using ATLAS-TCAD simulator. Energy band
diagram, doping profile, conduction current density,I-V caracteristic , internal potential and
electric field were performed.
Simulation of AlGaN/Si and InN/Si ELECTRIC –DEVICESijrap
In this work, efficient solar-blind metal-semiconductor photodetectors grown on Si (111) by
molecular beam epitaxy are reported. Growth details are described,the comparison enters the
properties electric of InN/Si and AlGaN/Si photodectors with 0.2 µm of AlGaN and InN layers.
Modeling and simulation were performed by using ATLAS-TCAD simulator. Energy band
diagram, doping profile, conduction current density,I-V caracteristic , internal potential and
electric field were performed
Similar to Uv spectroscopy 2019 part 2 compact (20)
Properties of coordination compounds part 1 (2018)Chris Sonntag
Using the crystal field theory, different properties of transition metal compounds can be explained, such as Ionic radii, hydration and lattice energies and spinel types
The Roman Empire A Historical Colossus.pdfkaushalkr1407
The Roman Empire, a vast and enduring power, stands as one of history's most remarkable civilizations, leaving an indelible imprint on the world. It emerged from the Roman Republic, transitioning into an imperial powerhouse under the leadership of Augustus Caesar in 27 BCE. This transformation marked the beginning of an era defined by unprecedented territorial expansion, architectural marvels, and profound cultural influence.
The empire's roots lie in the city of Rome, founded, according to legend, by Romulus in 753 BCE. Over centuries, Rome evolved from a small settlement to a formidable republic, characterized by a complex political system with elected officials and checks on power. However, internal strife, class conflicts, and military ambitions paved the way for the end of the Republic. Julius Caesar’s dictatorship and subsequent assassination in 44 BCE created a power vacuum, leading to a civil war. Octavian, later Augustus, emerged victorious, heralding the Roman Empire’s birth.
Under Augustus, the empire experienced the Pax Romana, a 200-year period of relative peace and stability. Augustus reformed the military, established efficient administrative systems, and initiated grand construction projects. The empire's borders expanded, encompassing territories from Britain to Egypt and from Spain to the Euphrates. Roman legions, renowned for their discipline and engineering prowess, secured and maintained these vast territories, building roads, fortifications, and cities that facilitated control and integration.
The Roman Empire’s society was hierarchical, with a rigid class system. At the top were the patricians, wealthy elites who held significant political power. Below them were the plebeians, free citizens with limited political influence, and the vast numbers of slaves who formed the backbone of the economy. The family unit was central, governed by the paterfamilias, the male head who held absolute authority.
Culturally, the Romans were eclectic, absorbing and adapting elements from the civilizations they encountered, particularly the Greeks. Roman art, literature, and philosophy reflected this synthesis, creating a rich cultural tapestry. Latin, the Roman language, became the lingua franca of the Western world, influencing numerous modern languages.
Roman architecture and engineering achievements were monumental. They perfected the arch, vault, and dome, constructing enduring structures like the Colosseum, Pantheon, and aqueducts. These engineering marvels not only showcased Roman ingenuity but also served practical purposes, from public entertainment to water supply.
Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
Palestine last event orientationfvgnh .pptxRaedMohamed3
An EFL lesson about the current events in Palestine. It is intended to be for intermediate students who wish to increase their listening skills through a short lesson in power point.
Operation “Blue Star” is the only event in the history of Independent India where the state went into war with its own people. Even after about 40 years it is not clear if it was culmination of states anger over people of the region, a political game of power or start of dictatorial chapter in the democratic setup.
The people of Punjab felt alienated from main stream due to denial of their just demands during a long democratic struggle since independence. As it happen all over the word, it led to militant struggle with great loss of lives of military, police and civilian personnel. Killing of Indira Gandhi and massacre of innocent Sikhs in Delhi and other India cities was also associated with this movement.
Synthetic Fiber Construction in lab .pptxPavel ( NSTU)
Synthetic fiber production is a fascinating and complex field that blends chemistry, engineering, and environmental science. By understanding these aspects, students can gain a comprehensive view of synthetic fiber production, its impact on society and the environment, and the potential for future innovations. Synthetic fibers play a crucial role in modern society, impacting various aspects of daily life, industry, and the environment. ynthetic fibers are integral to modern life, offering a range of benefits from cost-effectiveness and versatility to innovative applications and performance characteristics. While they pose environmental challenges, ongoing research and development aim to create more sustainable and eco-friendly alternatives. Understanding the importance of synthetic fibers helps in appreciating their role in the economy, industry, and daily life, while also emphasizing the need for sustainable practices and innovation.
The Indian economy is classified into different sectors to simplify the analysis and understanding of economic activities. For Class 10, it's essential to grasp the sectors of the Indian economy, understand their characteristics, and recognize their importance. This guide will provide detailed notes on the Sectors of the Indian Economy Class 10, using specific long-tail keywords to enhance comprehension.
For more information, visit-www.vavaclasses.com
We all have good and bad thoughts from time to time and situation to situation. We are bombarded daily with spiraling thoughts(both negative and positive) creating all-consuming feel , making us difficult to manage with associated suffering. Good thoughts are like our Mob Signal (Positive thought) amidst noise(negative thought) in the atmosphere. Negative thoughts like noise outweigh positive thoughts. These thoughts often create unwanted confusion, trouble, stress and frustration in our mind as well as chaos in our physical world. Negative thoughts are also known as “distorted thinking”.
Welcome to TechSoup New Member Orientation and Q&A (May 2024).pdfTechSoup
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Bills have a main role in point of sale procedure. It will help to track sales, handling payments and giving receipts to customers. Bill splitting also has an important role in POS. For example, If some friends come together for dinner and if they want to divide the bill then it is possible by POS bill splitting. This slide will show how to split bills in odoo 17 POS.
1. UV spectroscopy
for Nanoparticles and
TM complexes
Spectroscopic analysis Part 2
METAL NANOPARTICLES
SPR (Surface Plasmon Resonance)
https://www.sigmaaldrich.com/technical-documents/articles/materials-
science/nanomaterials/silver-nanoparticles.html
The strong interaction of the silver nanoparticles
with light occurs because the conduction
electrons on the metal surface undergo a
collective oscillation when excited by light at
specific wavelengths
Color (absorption maximum) corresponds to particle size.
Example: AgNP
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2. Applications of AgNP
Diagnostic Applications: Silver nanoparticles are used in biosensors and
numerous assays where the silver nanoparticle materials can be used as
biological tags for quantitative detection.
Antibacterial Applications: Silver nanoparticles are incorporated in
apparel, footwear, paints, wound dressings, appliances, cosmetics, and
plastics for their antibacterial properties.
Conductive Applications: Silver nanoparticles are used in conductive inks
and integrated into composites to enhance thermal and electrical
conductivity.
Optical Applications: Silver nanoparticles are used to efficiently harvest
light and for enhanced optical spectroscopies including metal-enhanced
fluorescence (MEF) and surface-enhanced Raman scattering (SERS).
Analyze these 4 samples of AgNP Influence of stabilizer
Reduction of AgNO3 by Na-citrate +/- PVP
No PVA + PVA
https://file.scirp.org/pdf/JMP_2015072215535041.pdf
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3. Number of atoms in one NP
d = diameter of NP
= density of the metal
M = molar mass of the metal
http://scholarcommons.usf.edu/ujmm/vol7/iss1/2/
Conc. of NP in “solution”
Lambert-Beer applied:
cf curcumin in DMSO: 5.54 * 104 M-1cm-1
Gold NP: max = 517 nm => = 1.1 * 10 7 (or 8 !?!) Estimation of particle size for AuNP
d = diameter of NP
0 = 512 nm
L1 = 6.53
L2 = 0.0216
https://pubs.acs.org/doi/pdf/10.1021/ac0702084
{for d > 25 nm)
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4. Alternative method using Absorption values:
Experimental parameters:
B1 = 3.00
B2 = 2.20
https://pubs.acs.org/doi/pdf/10.1021/ac0702084
COORDINATION COMPOUNDS
The electronic spectra of d-block complexes:
The features of electronic spectra that we need to be able to
master are:
1) naming of electronic states and d-d transitions,
e.g.3A2g, or 3A2g→1Eg
2) Explanation of relative intensities of bands in the
spectra of complexes of d-block metal ions.
(The Laporte and spin selection rules)
3) calculation of the crystal field splitting parameters from
energies of d-d bands
15
Introduction
d1 VIS Spectra
d1 Spectra 2
Composite Colors
16
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5. d-d spectra and MO theory:
3A2g →3T2g
3A2g →1Eg
υ, cm-1
UV
[Ni(NH3)6]2+
visible infrared
17
Naming of electronic states (1)
In names of electronic states, e.g. 4A2g, the labels A, E, and T,
stand for non-degenerate, doubly degenerate, and triply
degenerate, while the numeric superscript stands for the
multiplicity of the state, which is the number of unpaired
electrons plus one. Note that the electronic states can be
ground states (states of lowest energy) or excited states:
4A2g
t2g
eg
Multiplicity =
3 unpaired electrons + 1
= 4
Non-degenerate
ground state =
‘A’
g = gerade
energy
18
19
Naming of electronic states (2)
The suffixes are products of symmetry elements:
Products
https://www.webqc.org/symmetrypointgroup-oh.html
20
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6. eg
eg eg
t2g t2g
6A2g
3T2g
1A2g
Non-degenerate triply degenerate non-degenerate
Multiplicity
= 5 + 1
energy
t2g
Naming of electronic states (3)
NOTE: In determining degeneracy, one can re-arrange the electrons, but
the number of unpaired electrons must stay the same, and the number
of electrons in each of the eg and t2g levels must stay the same.
Multiplicity
= 2 + 1
Multiplicity
= 0 + 1 21
eg
eg eg
t2g t2g
5Eg
5T2g
2Eg
eg
eg eg
t2g t2g
3A2g
1Eg
3T2g
Naming of electronic states (contd.):
t2g
t2g
ground state excited state excited state
ground state excited state ground state
energy
22
Electronic Transitions
Example d2 complex
23
Electronic transitions for Ni2+
eg
eg
eg
eg
t2g t2g
t2g t2g
3A2g →3T2g
3A2g →1Eg
3A2g
3T2g
3A2g
1Eg
ground state excited state 24
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7. visible infraredUV
green
3A2g →3T2g
3A2g →1Eg
[Ni(H2O)6]2+
The electronic spectrum of [Ni(H2O)6]2+:
λ,
The complex looks green, because it absorbs only weakly at 500 nm,
the wavelength of green light.
25
On the previous slide we saw the two bands due to the 3A2g
→3T2g and 3A2g →1Eg transitions. The band at λ = 1180 nm
which is the 3A2g →3T2g transition shown below, corresponds
to Δ for the complex. This is usually expressed as Δ in cm-1 =
(1/λ(nm)) x 107 = 8500 cm-1.
The electronic spectrum of [Ni(H2O)6]2+:
eg
eg
t2g t2g
3A2g →3T2g3A2g
3T2gΔ
= Δ
= 8500
cm-1
26
Note the weak band at 620 nm that corresponds to the 3A2g
→1Eg transition. The electron that is excited moves within the
eg level, so that the energy does not involve Δ, but depends
on the value of P, the spin-pairing energy. The point of interest
is why this band is so weak, as discussed on the next slide.
The electronic spectrum of [Ni(H2O)6]2+:
eg
eg
t2g t2g
3A2g →1Eg3A2g
1EgΔ
= 16100
cm-1
27
The electronic spectrum of [Ni(H2O)6]2+:
The two peaks at higher energy resemble the 3A2g→3T2g transition, but
involve differences in magnetic quantum numbers of the d-orbitals,
and are labeled as 3A2g→3T1g(F) and 3A2g→3T1g(P) to reflect this:
3A2g →3T2g
3A2g →3T1g(F)
3A2g →3T1g(P)
3A2g →1Eg
λ,
[Ni(H2O)6]2+
28
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8. Selection Rules
29
1
30
All transitions within the d-shell, such as 3A2g→3T2g are Laporte
forbidden, because they are g→g. Thus, the intensity of the d-d
transitions that give d-block metal ions their colors are not very
intense.
Charge transfer bands frequently involve p→d or d→p transi ons,
and so are Laporte-allowed and therefore very intense.
2
31
The Selection rules for electronic transitions
3A2g →3T2g
Charge-transfer band – Laporte and spin allowed – very intense
[Ni(H2O)6]2+
a
b c
3A2g →1Eg Laporte and spin forbidden – very weak
a, b, and c, Laporte
forbidden, spin
allowed, inter-
mediate intensity
32
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9. The three types of bands present in e.g. [Ni(H2O)6]2+ are:
1) Laporte-allowed plus spin allowed charge transfer
bands of very high intensity
2) Laporte-forbidden plus spin-allowed d→d transi ons (e.g.
3A2g→3T2g) of moderate intensity
3) Laporte forbidden plus spin-forbidden d→d transi ons
(3A2g→1Eg) of very low intensity.
The Intensity of bands in complexes of d-block ions:
33
The MO view of electronic transitions in an octahedral
complex
t1u*
a1g*
eg*
t2g
t1u
eg
4p
4s
a1g
3d
t2g→t1u*
M→L Charge transfer
Laporte and spin
allowed
t1u→t2g
L→M Charge transfer
Laporte and spin
allowed
t2g→eg
d→d transition
Laporte forbidden
Spin-allowed or
forbidden
The eg level in CFT
is an eg* in MO
In CFT we consider
only the eg and t2g
levels, which are a
portion of the over-
all MO diagram
σ-donor orbitals
of six ligands
34
Charge-Transfer Peaks
Explanation and example for MnO4
-
35
There are two mechanisms that allow ‘forbidden’ electronic
transitions to become somewhat ‘allowed’. These are:
1) Mixing of states: The states in a complex are never pure,
and so some of the symmetry properties of neighboring states
become mixed into those of the states involved in a
‘forbidden’ transition.
2) Vibronic Coupling: Electronic states are always coupled to
vibrational states. The vibrational states may be of opposite
parity to the electronic states, and so help overcome the
Laporte selection rule.
Why do we see ‘forbidden’ transitions at all?
36
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10. Mixing of states: Comparison of [Ni(H2O)6]2+ and [Ni(en)3]2+:
[Ni(H2O)6]2+
[Ni(en)3]2+
3A2g →3T2g
3A2g →3T2g(F)
The spin-forbidden 3A2g →1Eg is close to the spin-allowed
3A2g →3T2g(F) and ‘borrows’ intensity by mixing of states
The spin-forbidden 3A2g →1Eg is not close
to any spin allowed band and is very weak
3A2g →1Eg
Note: The two spectra are
drawn on the same graph
for ease of comparison.
37
Electronic transitions are coupled to vibrations of various
symmetries, and the latter may impart opposite parity to an
electronic state and so help overcome the Laporte selection
rule:
Vibronic coupling:
electronic ground
state is ‘g’
electronic excited
state is ‘g’
g→g transition
is forbidden
g→(g+u) transition
is allowed
energy
coupled vibration
υ4’ is ‘u’
Electronic transitions, as seen
in the spectra of complexes of
Ni(II) shown above, are always
very broad because they are
coupled to vibrations. The
transitions are thus from ground
states plus several vibrational
states to excited states plus
several vibrational states (υ1, υ2, υ3),
so the ‘electronic’ band is actually
a composite of electronic plus
vibrational transitions.
υ5
υ3
υ1
υ5’
υ3’
υ1’
38
Symmetry of vibrational states, and their coupling to
electronic states:
T1u
symmetry
vibration
A1g
symmetry
vibration
(symbols have same meaning for
vibrations: A = non-degenerate,
T = triply degenerate, g = gerade,
u = ungerade, etc.)
The band one sees in the
UV-visible spectrum is the
sum of bands due to transitions
to coupled electronic (E) and
vibrational energy levels (υ1, υ2, υ3)
observed
spectrum
E E- υ1
E- υ2
E- υ3
E + υ1’
E + υ2’
E + υ3’
39
The spectra of high-spin d5 ions:
6A2g →4T2g
energy
For high-spin d5 ions all possible d-d transitions are spin-forbidden. As a
result, the bands in spectra of high-spin complexes of Mn(II) and Fe(III)
are very weak, and the compounds are nearly colorless. Below is shown
a d-d transition for a high-spin d5 ion, showing that it is spin-forbidden.
eg
eg
t2g t2g
Complexes of Gd(III) are colorless, while those of other lanthanide
M(III) ions are colored, except for La(III) and Lu(III). Why is this?
40
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11. Square Planar Complexes
Orbitals and Transitions
41
The spectra of complexes of tetrahedral metal
ions:
A tetrahedron has no center of symmetry, and so orbitals in such
symmetry cannot be gerade. Hence the d-levels in a tetrahedral
complex are e and t2, with no ‘g’ for gerade.
This largely overcomes the Laporte selection rules, so that
tetrahedral complexes tend to be very intense in color. Thus, we
see that dissolving CoCl2 in water produces a pale pink solution of
[Co(H2O)6]2+, but in alcohol tetrahedral [CoCl2(CH3CH2OH)2] forms,
which is a very intense blue color. This remarkable difference in
the spectra of octahedral and tetrahedral complexes is seen on
the next slide:
42
The spectra of octahedral [Co(H2O)6]2+ and tetrahedral
[CoCl4]2- ions:
[CoCl4]2-
[Co(H2O)6]2+
The spectra at left
show the very intense
d-d bands in the blue
tetrahedral complex
[CoCl4]2-, as compared
with the much weaker
band in the pink
octahedral complex
[Co(H2O)6]2+. This
difference arises
because the Td com-
plex has no center of
symmetry, helping to
overcome the g→g
Laporte selection rule.
43
TANABE-SUGANO DIAGRAMS
44
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12. Free ion
terms
Spin allowed
transitions
Example d2
45 46
Calculate o
Energy ratio from the
peaks
Find ratio in the diagram
=> o/B value
From the E/B and the
o/B value:
find B and o
o/B = 30 and E/B = 28
=> o = 30 * B = 30 * E/28 = 30 * 17200/28
18500 cm-1
47
Exercise: Cr3+
Estimate the wavenumbers of the 2 peaks and calculate o
from the Tanabe Sugano diagram
48
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13. Tanabe Sugano for d3
Estimate /B and E/B from the
Energy-relation of the 2 peaks in
the spectrum.
From there you can calculate the
parameter B and from there the
splitting energy o
49 50
(1) Ratio of peak energies: 31000/ 23000 = 1.4
51
(2) Find the ratio 1.4 in the diagram
The ratio 1.4 can be found for a line at
/B = 24
=> E/B = 34 and 24
B = E(1)/24 = 23000/24 = 960
= B * 24 = 23000 cm-1
52
Questions
Which electronic state is ground and excited state and what is the
name ?
Which transition is stronger and why ?
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14. 53
Why there are 2 different 3T2 excited state ?
Why are high-spin d5 complexes colorless ?
54
Why CoCl4
2- has a strong color but Co(H2O)6
2+
is nearly colorless ?
How can this be used in a practical application ?
End of UV/VIS Part 2
55
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