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Not to be confused with Iridium.
Indium,  49In
General properties
Name, symbol indium, In
Pronunciation /ˈɪndiəm/
Appearance silvery lustrous gray
Indium in the periodic table
Hydrogen (diatomic nonmetal)
Helium (noble gas)
Lithium (alkali metal)
Beryllium (alkaline earth metal)
Boron (metalloid)
Carbon (polyatomic nonmetal)
Nitrogen (diatomic nonmetal)
Oxygen (diatomic nonmetal)
Fluorine (diatomic nonmetal)
Neon (noble gas)
Sodium (alkali metal)
Magnesium (alkaline earth metal)
Aluminium (post-transition metal)
Silicon (metalloid)
Phosphorus (polyatomic nonmetal)
Sulfur (polyatomic nonmetal)
Chlorine (diatomic nonmetal)
Argon (noble gas)
Potassium (alkali metal)
Calcium (alkaline earth metal)
Scandium (transition metal)
Titanium (transition metal)
Vanadium (transition metal)
Chromium (transition metal)
Manganese (transition metal)
Iron (transition metal)
Cobalt (transition metal)
Nickel (transition metal)
Copper (transition metal)
Zinc (transition metal)
Gallium (post-transition metal)
Germanium (metalloid)
Arsenic (metalloid)
Selenium (polyatomic nonmetal)
Bromine (diatomic nonmetal)
Krypton (noble gas)
Rubidium (alkali metal)
Strontium (alkaline earth metal)
Yttrium (transition metal)
Zirconium (transition metal)
Niobium (transition metal)
Molybdenum (transition metal)
Technetium (transition metal)
Ruthenium (transition metal)
Rhodium (transition metal)
Palladium (transition metal)
Silver (transition metal)
Cadmium (transition metal)
Indium (post-transition metal)
Tin (post-transition metal)
Antimony (metalloid)
Tellurium (metalloid)
Iodine (diatomic nonmetal)
Xenon (noble gas)
Caesium (alkali metal)
Barium (alkaline earth metal)
Lanthanum (lanthanide)
Cerium (lanthanide)
Praseodymium (lanthanide)
Neodymium (lanthanide)
Promethium (lanthanide)
Samarium (lanthanide)
Europium (lanthanide)
Gadolinium (lanthanide)
Terbium (lanthanide)
Dysprosium (lanthanide)
Holmium (lanthanide)
Erbium (lanthanide)
Thulium (lanthanide)
Ytterbium (lanthanide)
Lutetium (lanthanide)
Hafnium (transition metal)
Tantalum (transition metal)
Tungsten (transition metal)
Rhenium (transition metal)
Osmium (transition metal)
Iridium (transition metal)
Platinum (transition metal)
Gold (transition metal)
Mercury (transition metal)
Thallium (post-transition metal)
Lead (post-transition metal)
Bismuth (post-transition metal)
Polonium (post-transition metal)
Astatine (metalloid)
Radon (noble gas)
Francium (alkali metal)
Radium (alkaline earth metal)
Actinium (actinide)
Thorium (actinide)
Protactinium (actinide)
Uranium (actinide)
Neptunium (actinide)
Plutonium (actinide)
Americium (actinide)
Curium (actinide)
Berkelium (actinide)
Californium (actinide)
Einsteinium (actinide)
Fermium (actinide)
Mendelevium (actinide)
Nobelium (actinide)
Lawrencium (actinide)
Rutherfordium (transition metal)
Dubnium (transition metal)
Seaborgium (transition metal)
Bohrium (transition metal)
Hassium (transition metal)
Meitnerium (unknown chemical properties)
Darmstadtium (unknown chemical properties)
Roentgenium (unknown chemical properties)
Copernicium (transition metal)
Ununtrium (unknown chemical properties)
Flerovium (post-transition metal)
Ununpentium (unknown chemical properties)
Livermorium (unknown chemical properties)
Ununseptium (unknown chemical properties)
Ununoctium (unknown chemical properties)


Atomic number (Z) 49
Group, block group 13, p-block
Period period 5
Element category   post-transition metal
Standard atomic weight (±) (Ar) 114.818(1)[1]
Electron configuration [Kr] 4d10 5s2 5p1
per shell
2, 8, 18, 18, 3
Physical properties
Phase solid
Melting point 429.7485 K ​(156.5985 °C, ​313.8773 °F)
Boiling point 2345 K ​(2072 °C, ​3762 °F)
Density near r.t. 7.31 g/cm3
when liquid, at m.p. 7.02 g/cm3
Triple point 429.7445 K, ​~1 kPa[2]
Heat of fusion 3.281 kJ/mol
Heat of vaporization 231.8 kJ/mol
Molar heat capacity 26.74 J/(mol·K)
vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k
at T (K) 1196 1325 1485 1690 1962 2340
Atomic properties
Oxidation states 3, 2, 1, −1, −2, −5[3] ​(an amphoteric oxide)
Electronegativity Pauling scale: 1.78
Ionization energies 1st: 558.3 kJ/mol
2nd: 1820.7 kJ/mol
3rd: 2704 kJ/mol
Atomic radius empirical: 167 pm
Covalent radius 142±5 pm
Van der Waals radius 193 pm
Crystal structure tetragonal
Tetragonal crystal structure for indium
Speed of sound thin rod 1215 m/s (at 20 °C)
Thermal expansion 32.1 µm/(m·K) (at 25 °C)
Thermal conductivity 81.8 W/(m·K)
Electrical resistivity 83.7 nΩ·m (at 20 °C)
Magnetic ordering diamagnetic[4]
Young's modulus 11 GPa
Mohs hardness 1.2
Brinell hardness 8.8–10.0 MPa
CAS Number 7440-74-6
Discovery Ferdinand Reich and Hieronymous Theodor Richter (1863)
First isolation Hieronymous Theodor Richter (1864)
Most stable isotopes of indium
iso NA half-life DM DE (MeV) DP
113In 4.28% (SF) <24.281
115In 95.72% 4.41×1014 y β 0.495 115Sn
Decay modes in parentheses are predicted, but have not yet been observed
| references

Indium is a chemical element with symbol In and atomic number 49. It is a post-transition metal that makes up 0.21 parts per million of the Earth's crust. Very soft and malleable, Indium has a melting point higher than sodium and gallium, but lower than lithium or tin. Ferdinand Reich and Hieronymous Theodor Richter discovered it with spectroscopy in 1863, naming it for the indigo blue line in its spectrum. It was isolated the next year.

Chemically, indium is similar to gallium and thallium, and it is largely intermediate between the two in terms of its properties.[5] It is a minor component in zinc sulfide ores and is produced as a byproduct of zinc refinement. It is most notably used in the semiconductor industry, in low-melting-point metal alloys such as solders, in soft-metal high-vacuum seals, and in the production of transparent conductive coatings of indium tin oxide (ITO) on glass. Indium has no biological role, though its compounds are somewhat toxic when injected into the bloodstream. Most occupational exposure is through ingestion, from which indium compounds are not absorbed well, and inhalation, from which they are moderately absorbed.



Indium wetting the glass surface of a test tube

Indium is a silvery-white, highly ductile post-transition metal with a bright luster.[6] It is so soft (Mohs hardness 1.2) that like sodium, it can be cut with a knife. It also leaves a visible line on paper.[7] It is a member of group 13 on the periodic table and its properties are mostly intermediate between its vertical neighbours gallium and thallium. Like tin, a high-pitched cry is heard when indium is bent – a crackling sound due to crystal twinning.[6] Like gallium, indium is able to wet glass. Like both, indium has a low melting point, 156.60 °C (313.88 °F); higher than its lighter homologue, gallium, but lower than its heavier homologue, thallium, and lower than tin.[8] The boiling point is 2072 °C (3762 °F), higher than that of thallium, but lower than gallium, conversely to the general trend of melting points, but similarly to the trends down the other post-transition metal groups because of the weakness of the metallic bonding with few electrons delocalized.[9]

The density of indium, 7.31 g/cm3, is also greater than gallium, but lower than thallium. Below the critical temperature, 3.41 K, indium becomes a superconductor. At standard temperature and pressure, indium crystallizes in the face-centered tetragonal crystal system in the space group I4/mmm (lattice parametersa = 325 pm, c = 495 pm):[8] this is a slightly distorted face-centered cubic structure, where each indium atom has four neighbours at 324 pm distance and eight neighbours slightly further (336 pm).[10]


Indium has 49 electrons, with an electronic configuration of [Kr]4d105s25p1. In compounds, indium most commonly donates the three outermost electrons to become indium(III), In3+. In some cases, the pair of 5s-electrons are not donated, resulting in indium(I), In+. The stabilization of the monovalent state is attributed to the inert pair effect, in which relativistic effects stabilize the 5s-orbital, observed in heavier elements. Thallium (indium's heavier homolog) shows an even stronger effect, causing oxidation to thallium(I) to be more probable than to thallium(III),[11] whereas gallium (indium's lighter homolog) commonly shows only the +3 oxidation state. Thus, although thallium(III) is a moderately strong oxidizing agent, indium(III) is not, and many indium(I) compounds are powerful reducing agents.[12] While the energy required to include the s-electrons in chemical bonding is lowest for indium among the group 13 metals, bond energies decrease down the group so that by indium, the energy released in forming two additional bonds and attaining the +3 state is not always enough to outweigh the energy needed to involve the 5s-electrons.[13] Indium(I) oxide and hydroxide are more basic and indium(III) oxide and hydroxide are more acidic.[13]

A number of standard electrode potentials, depending on the reaction under study,[14] are reported for indium, reflecting the decreased stability of the +3 oxidation state:[10]

−0.40 In2+ + e ↔ In+
−0.49 In3+ + e ↔ In2+
−0.443 In3+ + 2 e ↔ In+
−0.3382 In3+ + 3 e ↔ In
−0.14 In+ + e ↔ In

Indium metal does not react with water, but it is oxidized by stronger oxidizing agents such as halogens to give indium(III) compounds. It does not form a boride, silicide, or carbide, and the hydride InH3 has at best a transitory existence in ethereal solutions at low temperatures, being unstable enough to spontaneously polymerize without coordination.[12] Indium is rather basic in aqueous solution, showing only slight amphoteric characteristics, and unlike its lighter homologs aluminium and gallium, it is insoluble in aqueous alkaline solutions.[15]


Main article: Isotopes of indium

Indium has 39 known isotopes, ranging in mass number from 97 to 135. Only two isotopes occur naturally as primordial nuclides: indium-113, the only stable isotope, and indium-115, which has a half-life of 4.41×1014 years, four orders of magnitude greater than the age of the universe and nearly 50,000 times greater than that of natural thorium.[16] The half-life of 115In is very long because the beta decay to 115Sn is spin-forbidden.[17] Indium-115 makes up 95.7% of all indium. Indium is one of three known elements (the others being tellurium and rhenium) of which the stable isotope is less abundant in nature than the long-lived primordial radioisotopes.[18]

The stablest artificial isotope is indium-111, with a half-life of approximately 2.8 days. All other isotopes have half-lives shorter than 5 hours. Indium also has 47 meta states, among which indium-114m1 (half-life about 49.51 days) is the most stable, more stable than the ground state of any indium isotope other than the primordial. All decay by isomeric transition. The indium isotopes lighter than 115In predominantly decay through electron capture or positron emission to form cadmium isotopes, while the other indium isotopes from 115In and greater predominantly decay through beta minus decay to form tin isotopes.[16]



InCl3 (structure pictured) is a common compound of indium.

Indium(III) oxide, In2O3, forms when indium metal is burned in air or when the hydroxide or nitrate is heated.[19] In2O3 adopts a structure like alumina and is amphoteric, that is able to react with both acids and bases. Indium reacts with water to reproduce soluble indium(III) hydroxide, which is also amphoteric; with alkalis to produce indates(III); and with acids to produce indium(III) salts:

In(OH)3 + 3 HCl → InCl3 + 3 H2O

The analogous sesquichalcogenides with sulfur, selenium, and tellurium are also known.[20] Indium forms the expected trihalides. Chlorination, bromination, and iodination of In produce colorless InCl3, InBr3, and yellow InI3. The compounds are Lewis acids, somewhat akin to the better known aluminium trihalides. Again like the related aluminium compound, InF3 is polymeric.[21]

Direct reaction of indium with the pnictogens produces the gray or semimetallic III–V semiconductors. Many of them slowly decompose in moist air, necessitating careful storage of semiconductor compounds to prevent contact with the atmosphere. Indium nitride is readily attacked by acids and alkalis.[22]


Indium(I) compounds are not common. The chloride, bromide, and iodide are deeply colored, unlike the parent trihalides from which they are prepared. The fluoride is known only as an unstable gaseous compound.[23] Indium(I) oxide black powder is produced when indium(III) oxide decomposes upon heating to 700 °C.[19]

Other oxidation states[edit]

Less frequently, indium forms compounds in oxidation state +2 and even fractional oxidation states. Usually such materials feature In–In bonding, most notably in the halides In2X4 and [In2X6]2−,[24] and various subchalcogenides such as In4Se3.[25] Several other compounds are known to combine indium(I) and indium(III), such as InI6(InIIICl6)Cl3,[26] InI5(InIIIBr4)2(InIIIBr6),[27] InIInIIIBr4.[24]

Organoindium compounds[edit]

Organoindium compounds feature In–C bonds. Most are In(III) derivatives, but cyclopentadienylindium(I) is an exception. It was the first known organoindium(I) compound,[28] and is polymeric, consisting of zigzag chains of alternating indium atoms and cyclopentadienyl complexes.[29] Perhaps the best-known organoindium compound is trimethylindium, In(CH3)3, used to prepare certain semiconducting materials.[30][31]


In 1863, the German chemists Ferdinand Reich and Hieronymous Theodor Richter were testing ores from the mines around Freiberg, Saxony. They dissolved the minerals pyrite, arsenopyrite, galena and sphalerite in hydrochloric acid and distilled raw zinc chloride. Reich, who was color-blind, employed Richter as an assistant for detecting the colored spectral lines. Knowing that ores from that region sometimes contain thallium, they searched for the green thallium emission spectrum lines. Instead, they found a bright blue line. Because that blue line did not match any known element, they hypothesized a new element was present in the minerals. They named the element indium, from the indigo color seen in its spectrum, after the Latin indicum.[32][33][34][35]

Richter went on to isolate the metal in 1864.[36] An ingot of 0.5 kg (1.1 lb) was presented at the World Fair 1867.[37] Reich and Richter later fell out when the latter claimed to be the sole discoverer.[35]


yellow squares with red and blue arrows
The s-process acting in the range from silver to antimony

Indium is created by the long-lasting (up to thousands of years) s-process (slow neutron capture) in low-to-medium-mass stars (which range in mass between 0.6 and 10 solar masses). When a silver-109 atom (the isotope that comprises approximately half of all silver in existence) catches a neutron, it undergoes a beta decay to become cadmium-110. Capturing further neutrons, it becomes cadmium-115, which decays to indium-115 by another beta decay. This explains why the radioactive isotope is more abundant than the stable one.[38] The stable indium isotope, indium-113, is one of the p-nuclei, the origin of which is not fully understood; although indium-113 is known to be made directly in the s- and r-processes (rapid neutron capture), and also as the daughter of very long-lived cadmium-113, which has a half-life of about eight quadrillion years, this cannot account for all indium-113.[39][40]

In Earth's crust, indium occurs rarely as grains of free metal, too rare and small for commercial importance.[41] Indium is 68th most abundant element in Earth's crust at approximately 160 ppb, approximately as abundant as cadmium.[42] Fewer than 10 indium minerals are known and none occur in significant deposits. Two such are dzhalindite (In(OH)3) and indite (FeIn2S4).[43]

Indium tends to occur with zinc in sulfide minerals because the two elements have similar atomic radii and other chemical properties.[44] Based on the content of indium in zinc ore stocks, the worldwide reserve of economically viable indium is approximately 6,000 tonnes,[45] and the Royal Society of Chemistry holds as a serious risk that indium supplies may be exhausted within a century.[46] However, the Indium Corporation, the largest processor of indium, claims on the basis of increasing recovery yields during extraction, that recovery will be possible from a wider range of base metals (tin, copper, and other polymetallic deposits) and from new mining investments, and the long-term supply of indium is sustainable, reliable, and sufficient to meet increasing future demands.[47]


World production trend[48]

The lack of indium mineral deposits and the fact that indium is enriched in sulfidic lead, tin, copper, iron and predominately in zinc deposits, makes zinc and lead production the main source for indium. The indium is leached from slag and dust of zinc production. Further purification is done by electrolysis.[49] The exact process varies with the exact composition of the slag and dust.[6][37]

Indium is produced mainly from residues generated during zinc ore processing but is also found in iron, lead, and copper ores.[6] China is a leading producer of indium (390 tonnes in 2012), followed by Canada, Japan and South Korea with 70 tonnes each.[50] The Teck Cominco refinery in Trail, British Columbia, is a large single-source indium producer, with an output of 32.5 tonnes in 2005, 41.8 tonnes in 2004 and 36.1 tonnes in 2003. South American Silver Corporation's Malku Khota property in Bolivia is a large resource of indium with an indicated resource of 1,481 tonnes and inferred resource of 935 tonnes.[51] Adex Mining Inc.'s Mount Pleasant Mine in New Brunswick, Canada, holds some of the world's total known indium resources.[52]

The primary consumption of indium worldwide is LCD production. Worldwide production in 2007 was 475 tonnes per year from mining and a further 650 tonnes per year from recycling.[47] Demand has risen rapidly in recent years with the popularity of LCD computer monitors and television sets, which now account for 50% of indium consumption.[53] Increased manufacturing efficiency and recycling (especially in Japan) maintain a balance between demand and supply. According to the UNEP, indium's end-of-life recycling rate is less than 1%.[54] According to estimate, fewer than 14 years of indium supplies are left, based on current rates of extraction, demonstrating the need for additional recycling.[55]


A magnified image of an LCD screen showing RGB pixels. Individual transistors are seen as white dots in the bottom part.

In 1924, indium was found to have a valued property of stabilizing non-ferrous metals, and that became the first significant use for the element.[56] The first large-scale application for indium was coating bearings in high-performance aircraft engines during World War II, to protect against damage and corrosion; this is no longer a major use of the element.[49] New uses were found in fusible alloys, solders, and electronics. In the 1950s, tiny beads of indium were used for the emitters and collectors of PNP alloy-junction transistors. In the middle and late 1980s, the development of indium phosphide semiconductors and indium tin oxide thin films for liquid-crystal displays (LCD) aroused much interest. By 1992, the thin-film application had become the largest end use.[57][58]

Indium(III) oxide and indium tin oxide (ITO) are used as a transparent conductive coating on glass substrates in electroluminescent panels.[59] Indium tin oxide is used as a light filter in low-pressure sodium-vapor lamps. The infrared radiation is reflected back into the lamp, which increases the temperature within the tube and improves the performance of the lamp.[58]

Indium has many semiconductor-related applications. Some indium compounds, such as indium antimonide and indium phosphide,[60] are semiconductors with useful properties: one precursor is usually trimethylindium (TMI), which is also used as the semiconductor dopant in II–VI compound semiconductors.[61] InAs and InSb are used for low-temperature transistors and InP for high-temperature transistors.[49] The compound semiconductors InGaN and InGaP are used in light-emitting diodes (LEDs) and laser diodes.[62] Indium is used in photovoltaics as the semiconductor copper indium gallium selenide (CIGS), also called CIGS solar cells, a type of second-generation thin-film solar cell.[63] Indium is used in PNP bipolar junction transistors with germanium: when soldered at low temperature, indium does not stress the germanium.[49]

Ductile indium wire

Indium wire is used as a vacuum seal and a thermal conductor in cryogenics and ultra-high-vacuum applications, in such manufacturing applications as gaskets that deform to fill gaps.[64] Indium is an ingredient in the gallium–indium–tin alloy galinstan, which is liquid at room temperature and replaces mercury in some thermometers.[65] Other alloys of indium with bismuth, cadmium, lead, and tin, which have higher but still low melting points (between 50 and 100 °C), are used in fire sprinkler systems and heat regulators.[49]

Indium is one of many substitutes for mercury in alkaline batteries to prevent the zinc from corroding and releasing hydrogen gas.[66] Indium is added to some dental amalgam alloys to decrease the surface tension of the mercury and allow for less mercury and easier amalgamation.[67]

Indium's high neutron-capture cross-section for thermal neutrons makes it suitable for use in control rods for nuclear reactors, typically in an alloy of 80% silver, 15% indium, and 5% cadmium.[68] In nuclear engineering, the (n,n') reactions of 113In and 115In are used to determine magnitudes of neutron fluxes.[69]

Biological role and precautions[edit]

Indium has no metabolic role in any organism. In a similar way to aluminium salts, indium(III) ions can be toxic to the kidney when given by injection.[70] Indium tin oxide and indium phosphide harm the pulmonary and immune systems, predominantly through ionic indium,[71] though hydrated indium oxide is more than forty times as toxic when injected, measured by the quantity of indium introduced.[70] Radioactive indium-111 (in very small amounts on a chemical basis) is used in nuclear medicine tests, as a radiotracer to follow the movement of labeled proteins and white blood cells in the body.[72][73] Indium compounds are mostly not absorbed upon ingestion and are only moderately absorbed on inhalation; they tend to be stored temporarily in the muscles, skin, and bones before being excreted, and the biological half-life of indium is about two weeks in humans.[74]

People can be exposed to indium in the workplace by inhalation, ingestion, skin contact, and eye contact. The National Institute for Occupational Safety and Health has set a recommended exposure limit (REL) of 0.1 mg/m3 over an 8-hour workday.[75]

See also[edit]


  1. ^ Standard Atomic Weights 2013. Commission on Isotopic Abundances and Atomic Weights
  2. ^ Mangum, B W (1989). "Determination of the Indium Freezing-point and Triple-point Temperatures". Metrologia. 26 (4): 211. Bibcode:1989Metro..26..211M. doi:10.1088/0026-1394/26/4/001. 
  3. ^ Guloy, A. M.; Corbett, J. D. (1996). "Synthesis, Structure, and Bonding of Two Lanthanum Indium Germanides with Novel Structures and Properties". Inorganic Chemistry. 35 (9): 2616–22. doi:10.1021/ic951378e. 
  4. ^ Lide, D. R., ed. (2005). "Magnetic susceptibility of the elements and inorganic compounds". CRC Handbook of Chemistry and Physics (PDF) (86th ed.). Boca Raton (FL): CRC Press. ISBN 0-8493-0486-5. 
  5. ^ W. M. Haynes (2010). David R. Lide, ed. CRC Handbook of Chemistry and Physics: A Ready-reference Book of Chemical and Physical Data. CRC Press. ISBN 978-1-4398-2077-3. 
  6. ^ a b c d Alfantazi, A. M.; Moskalyk, R. R. (2003). "Processing of indium: a review". Minerals Engineering. 16 (8): 687–694. doi:10.1016/S0892-6875(03)00168-7. 
  7. ^ Binder, Harry H. (1999). Lexicon der chemischen Elemente (in German). S. Hirzel Verlag. ISBN 3-7776-0736-3. 
  8. ^ a b Dean, John A. (523). Lange's handbook of chemistry (Fifteenth edition). McGraw-Hill, Inc. ISBN 0-07-016190-9. 
  9. ^ Greenwood and Earnshaw, p. 222
  10. ^ a b Greenwood and Earnshaw, p. 252
  11. ^ Holleman, Arnold F.; Wiberg, Egon; Wiberg, Nils (1985). "Thallium". Lehrbuch der Anorganischen Chemie (in German) (91–100 ed.). Walter de Gruyter. pp. 892–893. ISBN 3-11-007511-3. 
  12. ^ a b Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 0-08-037941-9. 
  13. ^ a b Greenwood and Earnshaw, p. 256
  14. ^ Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 8.20. ISBN 1439855110. 
  15. ^ Greenwood and Earnshaw, p. 255
  16. ^ a b Audi, Georges; Bersillon, O.; Blachot, J.; Wapstra, A.H. (2003). "The NUBASE Evaluation of Nuclear and Decay Properties". Nuclear Physics A. Atomic Mass Data Center. 729: 3–128. Bibcode:2003NuPhA.729....3A. doi:10.1016/j.nuclphysa.2003.11.001. 
  17. ^ Dvornický, R.; Šimkovic, F. (13–16 June 2011). "Second unique forbidden β decay of 115In and neutrino mass". AIP Conf. Proc. 1417 (33). doi:10.1063/1.3671032. 
  18. ^ "IUPAC Periodic Table of the Isotopes" (PDF). IUPAC. 1 October 2013. Retrieved 21 June 2016. 
  19. ^ a b Anthony John Downs (1993). Chemistry of aluminium, gallium, indium, and thallium. Springer. ISBN 0-7514-0103-X. 
  20. ^ Greenwood and Earnshaw, p. 286
  21. ^ Greenwood and Earnshaw, pp. 263–7
  22. ^ Greenwood and Earnshaw, p. 288
  23. ^ Greenwood and Earnshaw, pp. 270–1
  24. ^ a b Sinclair, Ian; Worrall, Ian J. (1982). "Neutral complexes of the indium dihalides". Canadian Journal of Chemistry. 60 (6): 695–698. doi:10.1139/v82-102. 
  25. ^ Greenwood and Earnshaw, p. 287
  26. ^ Beck, Horst Philipp; Wilhelm, Doris (1991). "In7Cl9—A New"Old" Compound in the System In-Cl". Angewandte Chemie International Edition in English. 30 (7): 824–825. doi:10.1002/anie.199108241. 
  27. ^ Dronskowski, Richard (1995). "Synthesis, Structure, and Decay of In4Br7". Angewandte Chemie International Edition in English. 34 (10): 1126–1128. doi:10.1002/anie.199511261. 
  28. ^ Fischer, E. O.; Hofmann, H. P. (1957). "Metall-cyclopentadienyle des Indiums". Angewandte Chemie (in German). 69 (20): 639–640. doi:10.1002/ange.19570692008. 
  29. ^ Beachley O. T.; Pazik J. C.; Glassman T. E.; Churchill M. R.; Fettinger J.C.; Blom R. (1988). "Synthesis, characterization and structural studies of In(C5H4Me) by x-ray diffraction and electron diffraction techniques and a reinvestigation of the crystalline state of In(C5H5) by x-ray diffraction studies". Organometallics. 7 (5): 1051–1059. doi:10.1021/om00095a007. 
  30. ^ Shenai, Deo V.; Timmons, Michael L.; Dicarlo, Ronald L.; Lemnah, Gregory K.; Stennick, Robert S. (2003). "Correlation of vapor pressure equation and film properties with trimethylindium purity for the MOVPE grown III–V compounds". Journal of Crystal Growth. 248: 91. doi:10.1016/S0022-0248(02)01854-7. 
  31. ^ Shenai, Deodatta V.; Timmons, Michael L.; Dicarlo, Ronald L.; Marsman, Charles J. (2004). "Correlation of film properties and reduced impurity concentrations in sources for III/V-MOVPE using high-purity trimethylindium and tertiarybutylphosphine". Journal of Crystal Growth. 272: 603. doi:10.1016/j.jcrysgro.2004.09.006. 
  32. ^ Reich, F.; Richter, T. (1863). "Ueber das Indium". Journal für Praktische Chemie (in German). 90 (1): 172–176. doi:10.1002/prac.18630900122. 
  33. ^ Venetskii, S. (1971). "Indium". Metallurgist. 15 (2): 148–150. doi:10.1007/BF01088126. 
  34. ^ Greenwood and Earnshaw, p. 244
  35. ^ a b Weeks, Mary Elvira (1932). "The Discovery of the Elements: XIII. Some Spectroscopic Studies". Journal of Chemical Education. 9 (8): 1413–1434. Bibcode:1932JChEd...9.1413W. doi:10.1021/ed009p1413. 
  36. ^ Reich, F.; Richter, T. (1864). "Ueber das Indium". Journal für Praktische Chemie (in German). 92 (1): 480–485. doi:10.1002/prac.18640920180. 
  37. ^ a b Schwarz-Schampera, Ulrich; Herzig, Peter M. (2002). Indium: Geology, Mineralogy, and Economics. Springer. ISBN 978-3-540-43135-0. 
  38. ^ Boothroyd, A. I. (2006). "Heavy elements in stars". Science. 314 (5806): 1690–1691. doi:10.1126/science.1136842. PMID 17170281. 
  39. ^ C. Arlandini, F. Käppeler, K. Wisshak, R. Gallino, M. Lugaro, M. Busso, O. Straniero: Neutron Capture in Low-Mass Asymptotic Giant Branch Stars: Cross Sections and Abundance Signatures. In: The Astrophysical Journal, Vol. 525, 1999, p. 886–900. ( doi:10.1086/307938)
  40. ^ Zs. Nemeth, F. Käppeler, C. Theis, T. Belgya, S. W. Yates: Nucleosynthesis in the Cd-In-Sn region. In: The Astrophysical Journal, Vol. 426, 1994, p. 357–365. ( doi:10.1086/174071)
  41. ^ Hudson Institute of Mineralogy (1993–2016). "Indium". Retrieved 21 June 2016. 
  42. ^ "Abundance in Earth's Crust". Archived from the original on 9 March 2007. Retrieved 2007-04-14. 
  43. ^ Sutherland, J. K. (1971). "A second occurrence of dzhalindite". The Canadian Mineralogist. 10 (5): 781–786. 
  44. ^ Greenwood and Earnshaw, p. 246
  45. ^ "Mineral Commodities Summary 2007: Indium" (PDF). United States Geological Survey. Retrieved 2007-12-26. 
  46. ^ Davies, Emma (January 2011). "Endangered elements: critical thinking" (PDF). Chemistry World. Royal Society of Chemistry. 8 (1): 50–4. Retrieved 20 June 2016. 
  47. ^ a b "Indium and Gallium Supply Sustainability September 2007 Update". 22nd EU PV Conference, Milan, Italy. Archived from the original (PDF) on 28 December 2008. Retrieved 2007-12-26. 
  48. ^ U.S. Geological Survey – Historical Statistics for Mineral and Material Commodities in the United States; INDIUM STATISTICS // USGS, April 1, 2014
  49. ^ a b c d e Greenwood and Earnshaw, p. 247
  50. ^ Tolcin, Amy C. (2013) Indium. USGS Mineral Commodity Summaries.
  51. ^ "Malku Khota Updated Preliminary Economic Assessment, May 2011" (PDF). South American Silver Corp. Archived from the original (PDF) on 2012-01-19. 
  52. ^ Wright, Philip (1996). "Mineral and Metal Commodity Review: Tin" (PDF). Natural Resources Canada. [dead link]
  53. ^ "Indium Price Supported by LCD Demand and New Uses for the Metal" (PDF). Retrieved 2007-12-26. 
  54. ^ "USGS Mineral Commodity Summaries 2011" (PDF). USGS and USDI. Retrieved August 2, 2011. 
  55. ^ "How much is left?". ScientificAmerican. Retrieved 16 January 2013. 
  56. ^ French, Sidney J. (1934). "A story of indium". Journal of Chemical Education. 11 (5): 270. Bibcode:1934JChEd..11..270F. doi:10.1021/ed011p270. 
  57. ^ Tolcin, Amy C. "Mineral Yearbook 2007: Indium" (PDF). United States Geological Survey. 
  58. ^ a b Downs, Anthony John (1993). Chemistry of Aluminium, Gallium, Indium, and Thallium. Springer. pp. 89 and 106. ISBN 978-0-7514-0103-5. 
  59. ^ "The Electroluminescent Light Sabre". Nanotechnology News Archive. Azonano. June 2, 2005. Archived from the original on October 12, 2007. Retrieved 2007-08-29. 
  60. ^ Bachmann, K. J. (1981). "Properties, Preparation, and Device Applications of Indium Phosphide". Annual Review of Materials Science. 11: 441–484. Bibcode:1981AnRMS..11..441B. doi:10.1146/ 
  61. ^ Shenai, Deodatta V.; Timmons, Michael L.; DiCarlo Jr., Ronald L.; Marsman, Charles J. (2004). "Correlation of film properties and reduced impurity concentrations in sources for III/V-MOVPE using high-purity trimethylindium and tertiarybutylphosphine". Journal of Crystal Growth. 272 (1–4): 603–608. Bibcode:2004JCrGr.272..603S. doi:10.1016/j.jcrysgro.2004.09.006. 
  62. ^ Schubert, E. Fred (2003). Light-Emitting Diodes. Cambridge University Press. p. 16. ISBN 0-521-53351-1. 
  63. ^ Powalla, M.; Dimmler, B. (2000). "Scaling up issues of CIGS solar cells". Thin Solid Films. 361–362: 540–546. Bibcode:2000TSF...361..540P. doi:10.1016/S0040-6090(99)00849-4. 
  64. ^ Weissler, G. L., ed. (1990). "Vacuum physics and technology". San Diego: Acad. Press: 296. ISBN 978-0-12-475914-5. 
  65. ^ Surmann, P; Zeyat, H (Nov 2005). "Voltammetric analysis using a self-renewable non-mercury electrode". Analytical and Bioanalytical Chemistry. 383 (6): 1009–13. doi:10.1007/s00216-005-0069-7. PMID 16228199. 
  66. ^ Geological Survey (U.S.) (2010). Minerals Yearbook, 2008, V. 1, Metals and Minerals. Government Printing Office. pp. 35–2. ISBN 978-1-4113-3015-3. 
  67. ^ Powell L. V., Johnson G. H., Bales D. J. (1989). "Effect of Admixed Indium on Mercury Vapor Release from Dental Amalgam". Journal of Dental Research. 68 (8): 1231–3. doi:10.1177/00220345890680080301. PMID 2632609. 
  68. ^ Scoullos, Michael J. (2001-12-31). "Other types of cadmium alloys". Mercury, cadmium, lead: handbook for sustainable heavy metals policy and regulation. p. 222. ISBN 978-1-4020-0224-3. 
  69. ^ Berger, Harold; National Bureau Of Standards, United States; Committee E-7 On Nondestructive Testing, American Society for Testing and Materials (1976). "Image Detectors for Other Neutron Energies". Practical applications of neutron radiography and gaging: a symposium. pp. 50–51. 
  70. ^ a b Castronovo, F. P.; Wagner, H. N. (October 1971). "Factors Affecting the Toxicity of the Element Indium". British Journal of Experimental Pathology. 52 (5): 543–559. PMC 2072430free to read. 
  71. ^ Gwinn, W. M.; Qu, W; Bousquet, R. W.; Price, H; Shines, C. J.; Taylor, G. J.; Waalkes, M. P.; Morgan, D. L. (2014). "Macrophage Solubilization and Cytotoxicity of Indium-Containing Particles as in vitro Correlates to Pulmonary Toxicity in vivo". Toxicological Sciences. 144 (1): 17–26. doi:10.1093/toxsci/kfu273. PMC 4349143free to read. PMID 25527823. 
  72. ^ "IN-111 FACT SHEET" (PDF). Nordion(Canada), Inc. Retrieved 23 September 2012. 
  73. ^ Van Nostrand, D.; Abreu, S. H.; Callaghan, J. J.; Atkins, F. B.; Stoops, H. C.; Savory, C. G. (May 1988). "In-111-labeled white blood cell uptake in noninfected closed fracture in humans: prospective study". Radiology. 167 (2): 495–498. doi:10.1148/radiology.167.2.3357961. PMID 3357961. 
  74. ^ Nordberg, Gunnar F.; Fowler, Bruce A.; Nordberg, Monica (7 August 2014). Handbook on the Toxicology of Metals (4th ed.). Academic Press. p. 845. ISBN 978-0-12-397339-9. 
  75. ^ "CDC – NIOSH Pocket Guide to Chemical Hazards – Indium". Retrieved 2015-11-06. 


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