The color of chemicals is a physical property of chemicals that in most cases comes from the excitation of electrons due to an absorption of energy performed by the chemical.
The study of chemical structure by means of energy absorption and release is generally referred to as spectroscopy.
The Colour bond more than covalent more will the colour intensity...!! All atoms and molecules are capable of absorbing and releasing energy in the form of photons, accompanied by a change of quantum state. The amount of energy absorbed or released is the difference between the energies of the two quantum states. There are various types of quantum state, including, for example, the rotational and vibrational states of a molecule. However the release of energy visible to the human eye, commonly referred to as visible light, spans the wavelengths approximately 380 nm to 760 nm, depending on the individual, and photons in this range usually accompany a change in atomic or molecular orbital quantum state. The perception of light is governed by three types of color receptors in the eye, which are sensitive to different ranges of wavelength within this band.
The relationship between energy and wavelength is determined by the Planck-Einstein relation
where E is the energy of the quantum (photon), f is the frequency of the light wave, h is the Planck constant, λ is the wavelength and c is the speed of light.
The relationships between the energies of the various quantum states are treated by atomic orbital, molecular orbital, Ligand Field Theory and Crystal Field Theory. If photons of a particular wavelength are absorbed by matter, then when we observe light reflected from or transmitted through that matter, what we see is the complementary color, made up of the other visible wavelengths remaining. For example, beta-carotene has maximum absorption at 454 nm (blue light), consequently what visible light remains appears orange .
What is seen by the eye is not the color absorbed, but the complementary color from the removal of the absorbed wavelengths. This spectral perspective was first noted in atomic spectroscopy.
Below is a rough table of wavelengths, colors and complementary colors. This utilizes the scientific CMY and RGB color wheels rather than the traditional RYB color wheel. [1]
Wavelength (nm) | Color | Complementary color | ||
---|---|---|---|---|
400–424 | violet | yellow | ||
424–491 | blue | orange | ||
491–570 | green | red | ||
570–585 | yellow | violet | ||
585–647 | orange | blue | ||
647–700 | red | green |
This can only be used as a very rough guide, for instance if a narrow range of wavelengths within the band 647–700 nm is absorbed, then the blue and green receptors will be fully stimulated, making cyan, and the red receptor will be partially stimulated, diluting the cyan to a greyish hue.
The vast majority of simple inorganic (e.g. sodium chloride) and organic compounds (e.g. ethanol) are colorless. Transition metal compounds are often colored because of transitions of electrons between d-orbitals of different energy. (see Transition metal#Colored compounds). Organic compounds tend to be colored when there is extensive conjugation, causing the energy gap between the HOMO and LUMO to decrease, bringing the absorption band from the UV to the visible region. Similarly, color is due to the energy absorbed by the compound, when an electron transitions from the HOMO to the LUMO. Lycopene is a classic example of a compound with extensive conjugation (11 conjugated double bonds), giving rise to an intense red color (lycopene is responsible for the color of tomatoes). Charge-transfer complexes tend to have very intense colors for different reasons.
Name | Formula | Color | |
---|---|---|---|
Magnesium(II) | Mg2+ | colorless | |
Scandium(III) | Sc3+ | silver | |
Titanium(III) | Ti3+ | purple | |
Titanium(IV) | Ti4+ | silver | |
Titanyl | TiO2+ | colorless | |
Vanadium(II) | V2+ | light purple | |
Vanadium(III) | V3+ | dark grey-green | |
Vanadyl(IV) | VO2+ | blue | |
Vanadium(IV) (vanadite) | V 4O2− 9 | brown | |
Vanadium(V) (pervanadyl) | VO+ 2 | yellow | |
Metavanadate | VO− 3 | colorless | |
Orthovanadate | VO3− 4 | colorless | |
Chromium(II) | Cr2+ | bright blue | |
Chromium(III) | Cr3+ | blue-green-grey | |
Chromium(III) hydroxide | Cr(OH)63− | yellowish | |
Monochromate | CrO2− 4 | yellow | |
Dichromate | Cr 2O2− 7 | orange | |
Manganese(II) | Mn2+ | pale pink | |
Manganese(III) | Mn3+ | crimson | |
Manganate(V) | MnO3− 4 | deep blue | |
Manganate(VI) | MnO2− 4 | dark green | |
Manganate(VII) (permanganate) | MnO− 4 | deep purple | |
Iron(II) | Fe2+ | greenish | |
Cobalt(II) fluoride | Co2+ | pink | |
Cobalt(III) amine | Co(NH 3)3+ 6 | yellow/orange | |
Nickel(II) | Ni2+ | light green | |
Nickel(II) amine complex | Ni(NH 3)2+ 6 | lavender/blue | |
Copper(I) amine complex | Cu(NH 3)+ 2 | colorless | |
Copper(II) | Cu2+ | blue | |
Copper(II) amine complex | Cu(NH 3)2+ 4 | indigo-blue | |
Copper(II) chloride | CuCl2− 4 | blue-green | |
Zinc(II) | Zn2+ | colorless | |
Silver(I) | Ag+ | colorless | |
Silver(III) in conc. HNO3 | Ag3+ | dark brown |
However, elemental colors will vary depending on what they are complexed with, often as well as their chemical state. An example with vanadium(III); VCl3 has a distinctive reddish hue, whilst V2O3 appears black.
Predicting the color of a compound can be extremely complicated. Some examples include:
Name | Formula of the corresponding salts | Color | Picture |
---|---|---|---|
Iron(III) chloride hexahydrate | FeCl3·6H2O | yellow/brown | |
Iron(III) chloride anhydrate | FeCl3 | black | |
Chromium (III) sulfate | Cr2(SO4)3 | dark green | |
Copper(II) sulfate anhydrate | CuSO4 | white | |
Copper(II) sulfate pentahydrate | CuSO4·5H2O | blue | |
Copper(II) benzoate | Cu(C7H5O2)2 | blue | |
Cobalt(II) chloride | CoCl2 | dep blue | |
Cobalt(II) chloride hexahydrate | CoCl2·6H2O | deep magenta | |
Manganese(II) chloride tetrahydrate | MnCl2·4H2O | pink | |
Copper(II) chloride dihydrate | CuCl2·2H2O | blue-green | |
Nickel(II) chloride hexahydrate | NiCl2·6H2O | green | |
Lead(II) iodide | PbI2 | yellow | |
Ammonium dichromate | (NH4)2Cr2O7 | orange |
Name | Formula | Color | |
---|---|---|---|
Lithium | Li | red | |
Sodium | Na | yellow/orange | |
Magnesium | Mg | brilliant white | |
Potassium | K | lilac/violet | |
Calcium | Ca | brick red | |
Rubidium | Rb | red-violet | |
Strontium | Sr | red | |
Caesium | Cs | light blue | |
Barium | Ba | green/yellow | |
Copper | Cu | Blue/Green(Often with white flashes) | |
Lead | Pb | Grey/White |
Name | Formula | Color | |
---|---|---|---|
Hydrogen | H2 | colorless | |
Oxygen | O2 | pale blue | |
Ozone | O3 | pale blue | |
Fluorine | F2 | pale yellow | |
Chlorine | Cl2 | greenish yellow | |
Bromine | Br2 | red/brown | |
Iodine | I2 | dark purple | |
Chlorine dioxide | ClO2 | intense yellow | |
Dichlorine monoxide | Cl2O | brown/yellow | |
Nitrogen dioxide | NO2 | dark brown | |
Trifluoronitrosomethane | CF3NO | deep blue | |
Diazomethane | CH2N2 | yellow |
A variety of colors, often similar to the colors found in a flame test, are produced in a bead test, which is a qualitative test for determining metals. A platinum loop is moistened and dipped in a fine powder of the substance in question and borax. The loop with the adhered powders is then heated in a flame until it fuses and the color of the resulting bead observed.
Metal [3] | Oxidizing flame | Reducing flame |
---|---|---|
Aluminum | colorless (hot and cold), opaque | colorless, opaque |
Antimony | colorless, yellow or brown (hot) | gray and opaque |
Barium | colorless | |
Bismuth | colorless, yellow or brownish (hot) | gray and opaque |
Cadmium | colorless | gray and opaque |
Calcium | colorless | |
Cerium | red (hot) | colorless (hot and cold) |
Chromium | dark yellow (hot), green (cold) | green (hot and cold) |
Cobalt | blue (hot and cold) | blue (hot and cold) |
Copper | green (hot), blue (cold) | red, opaque (cold), colorless (hot) |
Gold | golden (hot), silver (cold) | red (hot and cold) |
Iron | yellow or brownish red (hot and cold) | green (hot and cold) |
Lead | colorless, yellow or brownish (hot) | gray and opaque |
Magnesium | colorless | |
Manganese | violet (hot and cold) | colorless (hot and cold) |
Molybdenum | colorless | yellow or brown (hot) |
Nickel | brown, red (cold) | gray and opaque (cold) |
Silicon | colorless (hot and cold), opaque | colorless, opaque |
Silver | colorless | gray and opaque |
Strontium | colorless | |
Tin | colorless (hot and cold), opaque | colorless, opaque |
Titanium | colorless | yellow (hot), violet (cold) |
Tungsten | colorless | brown |
Uranium | yellow or brownish (hot) | green |
Vanadium | colorless | green |
The electromagnetic spectrum is the full range of electromagnetic radiation, organized by frequency or wavelength. The spectrum is divided into separate bands, with different names for the electromagnetic waves within each band. From low to high frequency these are: radio waves, microwaves, infrared, visible light, ultraviolet, X-rays, and gamma rays. The electromagnetic waves in each of these bands have different characteristics, such as how they are produced, how they interact with matter, and their practical applications.
Fluorescence is one of two kinds of emission of light by a substance that has absorbed light or other electromagnetic radiation. When exposed to ultraviolet radiation, many substances will glow (fluoresce) with colored visible light. The color of the light emitted depends on the chemical composition of the substance. Fluorescent materials generally cease to glow nearly immediately when the radiation source stops. This distinguishes them from the other type of light emission, phosphorescence. Phosphorescent materials continue to emit light for some time after the radiation stops.
Spectroscopy is the field of study that measures and interprets electromagnetic spectrum. In narrower contexts, spectroscopy is the precise study of color as generalized from visible light to all bands of the electromagnetic spectrum.
A quantum mechanical system or particle that is bound—that is, confined spatially—can only take on certain discrete values of energy, called energy levels. This contrasts with classical particles, which can have any amount of energy. The term is commonly used for the energy levels of the electrons in atoms, ions, or molecules, which are bound by the electric field of the nucleus, but can also refer to energy levels of nuclei or vibrational or rotational energy levels in molecules. The energy spectrum of a system with such discrete energy levels is said to be quantized.
In theoretical chemistry, a conjugated system is a system of connected p-orbitals with delocalized electrons in a molecule, which in general lowers the overall energy of the molecule and increases stability. It is conventionally represented as having alternating single and multiple bonds. Lone pairs, radicals or carbenium ions may be part of the system, which may be cyclic, acyclic, linear or mixed. The term "conjugated" was coined in 1899 by the German chemist Johannes Thiele.
The emission spectrum of a chemical element or chemical compound is the spectrum of frequencies of electromagnetic radiation emitted due to electrons making a transition from a high energy state to a lower energy state. The photon energy of the emitted photons is equal to the energy difference between the two states. There are many possible electron transitions for each atom, and each transition has a specific energy difference. This collection of different transitions, leading to different radiated wavelengths, make up an emission spectrum. Each element's emission spectrum is unique. Therefore, spectroscopy can be used to identify elements in matter of unknown composition. Similarly, the emission spectra of molecules can be used in chemical analysis of substances.
In the field of optics, transparency is the physical property of allowing light to pass through the material without appreciable scattering of light. On a macroscopic scale, the photons can be said to follow Snell's law. Translucency allows light to pass through but does not necessarily follow Snell's law; the photons can be scattered at either of the two interfaces, or internally, where there is a change in the index of refraction. In other words, a translucent material is made up of components with different indices of refraction. A transparent material is made up of components with a uniform index of refraction. Transparent materials appear clear, with the overall appearance of one color, or any combination leading up to a brilliant spectrum of every color. The opposite property of translucency is opacity. Other categories of visual appearance, related to the perception of regular or diffuse reflection and transmission of light, have been organized under the concept of cesia in an order system with three variables, including transparency, translucency and opacity among the involved aspects.
Photochemistry is the branch of chemistry concerned with the chemical effects of light. Generally, this term is used to describe a chemical reaction caused by absorption of ultraviolet, visible (400–750 nm), or infrared radiation (750–2500 nm).
In physics, atomic spectroscopy is the study of the electromagnetic radiation absorbed and emitted by atoms. Since unique elements have unique emission spectra, atomic spectroscopy is applied for determination of elemental compositions. It can be divided by atomization source or by the type of spectroscopy used. In the latter case, the main division is between optical and mass spectrometry. Mass spectrometry generally gives significantly better analytical performance, but is also significantly more complex. This complexity translates into higher purchase costs, higher operational costs, more operator training, and a greater number of components that can potentially fail. Because optical spectroscopy is often less expensive and has performance adequate for many tasks, it is far more common. Atomic absorption spectrometers are one of the most commonly sold and used analytical devices.
Spectrophotometry is a branch of electromagnetic spectroscopy concerned with the quantitative measurement of the reflection or transmission properties of a material as a function of wavelength. Spectrophotometry uses photometers, known as spectrophotometers, that can measure the intensity of a light beam at different wavelengths. Although spectrophotometry is most commonly applied to ultraviolet, visible, and infrared radiation, modern spectrophotometers can interrogate wide swaths of the electromagnetic spectrum, including x-ray, ultraviolet, visible, infrared, and/or microwave wavelengths.
A chromophore is a molecule which absorbs light at a particular wavelength and reflects color as a result. Chromophores are commonly referred to as colored molecules for this reason. The word is derived from Ancient Greek χρῶμᾰ (chroma) 'color' and -φόρος (phoros) 'carrier of'. Many molecules in nature are chromophores, including chlorophyll, the molecule responsible for the green colors of leaves. The color that is seen by our eyes is that of the light not absorbed by the reflecting object within a certain wavelength spectrum of visible light. The chromophore indicates a region in the molecule where the energy difference between two separate molecular orbitals falls within the range of the visible spectrum. Visible light that hits the chromophore can thus be absorbed by exciting an electron from its ground state into an excited state. In biological molecules that serve to capture or detect light energy, the chromophore is the moiety that causes a conformational change in the molecule when hit by light.
The color of water varies with the ambient conditions in which that water is present. While relatively small quantities of water appear to be colorless, pure water has a slight blue color that becomes deeper as the thickness of the observed sample increases. The hue of water is an intrinsic property and is caused by selective absorption and scattering of blue light. Dissolved elements or suspended impurities may give water a different color.
In theoretical chemistry, molecular electronic transitions take place when electrons in a molecule are excited from one energy level to a higher energy level. The energy change associated with this transition provides information on the structure of the molecule and determines many of its properties, such as colour. The relationship between the energy involved in the electronic transition and the frequency of radiation is given by Planck's relation.
Photosensitizers are light absorbers that alter the course of a photochemical reaction. They usually are catalysts. They can function by many mechanisms, sometimes they donate an electron to the substrate, sometimes they abstract a hydrogen atom from the substrate. At the end of this process, the photosensitizer returns to its ground state, where it remains chemically intact, poised to absorb more light. One branch of chemistry which frequently utilizes photosensitizers is polymer chemistry, using photosensitizers in reactions such as photopolymerization, photocrosslinking, and photodegradation. Photosensitizers are also used to generate prolonged excited electronic states in organic molecules with uses in photocatalysis, photon upconversion and photodynamic therapy. Generally, photosensitizers absorb electromagnetic radiation consisting of infrared radiation, visible light radiation, and ultraviolet radiation and transfer absorbed energy into neighboring molecules. This absorption of light is made possible by photosensitizers' large de-localized π-systems, which lowers the energy of HOMO and LUMO orbitals to promote photoexcitation. While many photosensitizers are organic or organometallic compounds, there are also examples of using semiconductor quantum dots as photosensitizers.
The emission spectrum of atomic hydrogen has been divided into a number of spectral series, with wavelengths given by the Rydberg formula. These observed spectral lines are due to the electron making transitions between two energy levels in an atom. The classification of the series by the Rydberg formula was important in the development of quantum mechanics. The spectral series are important in astronomical spectroscopy for detecting the presence of hydrogen and calculating red shifts.
Photoexcitation is the production of an excited state of a quantum system by photon absorption. The excited state originates from the interaction between a photon and the quantum system. Photons carry energy that is determined by the wavelengths of the light that carries the photons. Objects that emit light with longer wavelengths, emit photons carrying less energy. In contrast to that, light with shorter wavelengths emit photons with more energy. When the photon interacts with a quantum system, it is therefore important to know what wavelength one is dealing with. A shorter wavelength will transfer more energy to the quantum system than longer wavelengths.
Photodissociation, photolysis, photodecomposition, or photofragmentation is a chemical reaction in which molecules of a chemical compound are broken down by absorption of light or photons. It is defined as the interaction of one or more photons with one target molecule that dissociates into two fragments.
Colored fire is a common pyrotechnic effect used in stage productions, fireworks and by fire performers the world over. Generally, the color of a flame may be red, orange, blue, yellow, or white, and is dominated by blackbody radiation from soot and steam. When additional chemicals are added to the fuel burning, their atomic emission spectra can affect the frequencies of visible light radiation emitted - in other words, the flame appears in a different color dependent upon the chemical additives. Flame coloring is also a good way to demonstrate how fire changes when subjected to heat and how they also change the matter around them.
Core electrons are the electrons in an atom that are not valence electrons and do not participate directly in chemical bonding. The nucleus and the core electrons of an atom form the atomic core. Core electrons are tightly bound to the nucleus. Therefore, unlike valence electrons, core electrons play a secondary role in chemical bonding and reactions by screening the positive charge of the atomic nucleus from the valence electrons.
Photoelectrochemical processes are processes in photoelectrochemistry; they usually involve transforming light into other forms of energy. These processes apply to photochemistry, optically pumped lasers, sensitized solar cells, luminescence, and photochromism.