Names | |
---|---|
Other names Cadmium(II) tetrafluoroborate Cadmium fluoroborate Cadmium fluoborate | |
Identifiers | |
3D model (JSmol) | |
ECHA InfoCard | 100.034.975 |
PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
| |
| |
Properties | |
Cd(BF4)2 | |
Molar mass | 286.020 g/mol |
Appearance | colorless solid crystals very hygroscopic |
Odor | odorless |
Density | 1.60 g/cm3 [1] |
very soluble | |
Solubility | very soluble in alcohol |
Hazards | |
NIOSH (US health exposure limits): | |
PEL (Permissible) | [1910.1027] TWA 0.005 mg/m3 (as Cd) [2] |
REL (Recommended) | Ca [2] |
IDLH (Immediate danger) | Ca [9 mg/m3 (as Cd)] [2] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Cadmium tetrafluoroborate is an ionic, chemical compound with the formula Cd(BF4)2. [3] It is a crystalline solid, which is colorless and odorless. Cadmium tetrafluoroborate is most frequently used in the industrial production of high-strength steels, its purpose being to prevent hydrogen absorption, a source of post-production cracking of the metal, in the treated steels. Another application of the chemistry of cadmium tetrafluoroborate is fine tuning of the size of cadmium telluride nanomaterials.
While the use of cadmium tetrafluoroborate is limited, concerns about limited or chronic exposure to this substance should be brought to the attention of a physician or other trained medical staff. Exposure to cadmium tetrafluoroborate, via ingestion, contact with the skin or mucous membranes, or inhalation can have lasting and harmful health effects.
Cadmium tetrafluoroborate may be prepared from the reaction between an aqueous solution of fluoroboric acid and cadmium carbonate or cadmium oxide: [4]
It is also possible to prepare cadmium tetrafluoroborate through an oxidation-reduction reaction implementing nitrosyl tetrafluoroborate: [5]
Cadmium tetrafluoroborate is an ionic compound formed from the two, ionic species Cd2+ and BF4−. At room temperature it forms colorless, odorless crystals which are soluble in polar solvents such as water or ethanol. At room temperature, the hydrated salt, Cd(BF4)2·6H2O, exists in a monoclinic crystal system, though this is temperature dependent. [6] Two, first-order phase transitions have been noted in the literature for this material, one each at 324 K and 177 K, representing a change in the crystal system from monoclinic to trigonal and from trigonal to either monoclinic or triclinic, respectively. [6] The quasi-trigonal geometry of the cadmium tetrafluoroborate hexahydrate crystal is unique among the first-row transition metal tetrafluoroborates and perchlorates, which have predominately hexagonal structures. [7]
The Cd2+ species of cadmium tetrafluoroborate may associate with various ligands to form transition-metal complexes. The structural formulas and geometries for such complexes can vary depending upon coordination number of the complex and the electronic properties of the ligands (see also, HSAB theory). However, two general forms may predominate: (i) [Cd(L)n(BF4)m], where L and BF4− are ligands in the inner-sphere, and (ii) [Cd(L)n](BF4)2, where BF4− is located in the outer-sphere; [8] for both, n=1,2,…,6. The literature contains reports of distorted octahedral geometries [9] [10] for Cadmium tetrafluoroborate complexes with nitrogen-containing ligands such as pyrazoles and imidazoles [9] and porphyrins. [10] Given the structural formulas for Cadmium tetrafluoroborate complexes noted in the literature [8] however, such as [Cd(L)4(BF4)2], it is likely that tetrahedral geometries are also possible in such complexes.
The most significant, industrial use of Cd(BF4)2 is in the electroplating of high-strength steels. [11] Here, species such as cadmium tetrafluoroborate (or Cd-Ti or CdCN) are deposited on the surface of steels in an electroplating process which inhibits absorption of hydrogen onto the surface of the steels, a source of cracking following baking of the metal. [11] Optimization of the electroplating process, adjusting electrolyte concentrations in Cadmium tetrafluoroborate mixes, has been explored in the literature. [12] Among other methods of electroplating, cadmium tetrafluoroborate baths have middling efficiency. It has, for instance, been demonstrated that traditional cyanide bathes (e.g. CdCN or ZnCN) and variants there-of provide more efficient distribution of current density during electroplating, resulting in steels which could bear greater loads. [13]
A method of etching of CdTe nanocrystals which removes Cd from the surface of the nano-structures via attack by tetrafluoroborate anions has been reported in the literature. [14] While the presence of Cd-F surface bonds and dissociation of Cd from the surface of the nano-structures are clear from the investigation, complex formation of Cd with BF4− in solution was not discussed though may be inferred from the spectrophotometric results. [14]
Methodology has been reported for the determination of boron concentration in steels using cadmium tetrafluoroborate complex formation during solvent extraction to facilitate indirect atomic absorption measurements. [15] Tetrafluoroborate, formed from acid extraction of boron for a steel sample using boric acid, associates with a transition metal complex of Cd2+ and forms a complex which is measureable by atomic absorption spectroscopy. [15] Similar procedures have been implemented for the same purpose using other transition metals [16] and for determination of boron in high-purity silicon using other cadmium tetrafluoroborate transition metal complexes. [17]
Cadmium tetreafluoroborate is a caustic substance, particularly when in aqueous solution. Multiple routes of exposure, such as ingestion, inhalation, or contact with the skin or mucous membranes, are available through contact with aqueous cadmium tetrafluorobromate. [18] [19] Target biological systems following exposure include the lungs, kidneys, and liver. [18] [19] Symptoms of cadmium tetrafluoroborate exposure include nausea, vomiting, fever, irritation of the mucous membranes (e.g. upper respiratory tract, eyes) and skin, coughing, wheezing, or difficulty breathing. [18] The mechanism of toxicity of this substance is related to cadmium poisoning and exposure to borates and hydrofluoric acid. [19] The compound functions in solution as a weakly acidic inorganic salt, neutralizing bases. [20] After initial exposure, thorough rising of the affected area with water is recommended. However, seeking medical attention is strongly advised as treatment for exposure to Cd or F containing compounds such as cadmium tetrafluoroborate generally involves intravenous administration (I.V.) of calcium chloride and sodium bicarbonate for the purpose of maintaining blood pH and sequestering Cd2+ and BF4− in insoluble salts. [19]
Chronic exposure to this substance may have negative health consequences. According to its OSHA, IARC, and ACGIH ratings, cadmium tetrafluoroborate is recognized as a carcinogenic substance. [11] [19] [21] [22] Further effects of chronic exposure may include hypocalcaemia and edemas of the respiratory system. [18]
Although this compound is a negligible fire hazard, [23] combustion of cadmium tetrafluoroborate produces hazardous decomposition products including cadmium/cadmium oxide and hydrogen fluoride. Therefore, cadmium tetrafluoroborate is stored out of direct light, in a cool environment, and away from other flammable materials.
Cadmium is a chemical element with the symbol Cd and atomic number 48. This soft, silvery-white metal is chemically similar to the two other stable metals in group 12, zinc and mercury. Like zinc, it demonstrates oxidation state +2 in most of its compounds, and like mercury, it has a lower melting point than the transition metals in groups 3 through 11. Cadmium and its congeners in group 12 are often not considered transition metals, in that they do not have partly filled d or f electron shells in the elemental or common oxidation states. The average concentration of cadmium in Earth's crust is between 0.1 and 0.5 parts per million (ppm). It was discovered in 1817 simultaneously by Stromeyer and Hermann, both in Germany, as an impurity in zinc carbonate.
A coordination complex consists of a central atom or ion, which is usually metallic and is called the coordination centre, and a surrounding array of bound molecules or ions, that are in turn known as ligands or complexing agents. Many metal-containing compounds, especially those that include transition metals, are coordination complexes.
Organometallic chemistry is the study of organometallic compounds, chemical compounds containing at least one chemical bond between a carbon atom of an organic molecule and a metal, including alkali, alkaline earth, and transition metals, and sometimes broadened to include metalloids like boron, silicon, and selenium, as well. Aside from bonds to organyl fragments or molecules, bonds to 'inorganic' carbon, like carbon monoxide, cyanide, or carbide, are generally considered to be organometallic as well. Some related compounds such as transition metal hydrides and metal phosphine complexes are often included in discussions of organometallic compounds, though strictly speaking, they are not necessarily organometallic. The related but distinct term "metalorganic compound" refers to metal-containing compounds lacking direct metal-carbon bonds but which contain organic ligands. Metal β-diketonates, alkoxides, dialkylamides, and metal phosphine complexes are representative members of this class. The field of organometallic chemistry combines aspects of traditional inorganic and organic chemistry.
Cadmium sulfate is the name of a series of related inorganic compounds with the formula CdSO4·xH2O. The most common form is the monohydrate CdSO4·H2O, but two other forms are known CdSO4·8⁄3H2O and the anhydrous salt (CdSO4). All salts are colourless and highly soluble in water.
Boron trifluoride is the inorganic compound with the formula BF3. This pungent, colourless, and toxic gas forms white fumes in moist air. It is a useful Lewis acid and a versatile building block for other boron compounds.
Cadmium chloride is a white crystalline compound of cadmium and chloride, with the formula CdCl2. This salt is a hygroscopic solid that is highly soluble in water and slightly soluble in alcohol. The crystal structure of cadmium chloride (described below), is a reference for describing other crystal structures. Also known are CdCl2•H2O and CdCl2•5H2O.
Anions that interact weakly with cations are termed non-coordinating anions, although a more accurate term is weakly coordinating anion. Non-coordinating anions are useful in studying the reactivity of electrophilic cations. They are commonly found as counterions for cationic metal complexes with an unsaturated coordination sphere. These special anions are essential components of homogeneous alkene polymerisation catalysts, where the active catalyst is a coordinatively unsaturated, cationic transition metal complex. For example, they are employed as counterions for the 14 valence electron cations [(C5H5)2ZrR]+ (R = methyl or a growing polyethylene chain). Complexes derived from non-coordinating anions have been used to catalyze hydrogenation, hydrosilylation, oligomerization, and the living polymerization of alkenes. The popularization of non-coordinating anions has contributed to increased understanding of agostic complexes wherein hydrocarbons and hydrogen serve as ligands. Non-coordinating anions are important components of many superacids, which result from the combination of Brønsted acids and Lewis acids.
Tin(II) chloride, also known as stannous chloride, is a white crystalline solid with the formula SnCl2. It forms a stable dihydrate, but aqueous solutions tend to undergo hydrolysis, particularly if hot. SnCl2 is widely used as a reducing agent (in acid solution), and in electrolytic baths for tin-plating. Tin(II) chloride should not be confused with the other chloride of tin; tin(IV) chloride or stannic chloride (SnCl4).
A salt metathesis reaction, sometimes called a double displacement reaction, is a chemical process involving the exchange of bonds between two reacting chemical species which results in the creation of products with similar or identical bonding affiliations. This reaction is represented by the general scheme:
Tetrafluoroborate is the anion BF−
4. This tetrahedral species is isoelectronic with tetrafluoroberyllate (BeF2−
4), tetrafluoromethane (CF4), and tetrafluoroammonium (NF+
4) and is valence isoelectronic with many stable and important species including the perchlorate anion, ClO−
4, which is used in similar ways in the laboratory. It arises by the reaction of fluoride salts with the Lewis acid BF3, treatment of tetrafluoroboric acid with base, or by treatment of boric acid with hydrofluoric acid.
Cadmium oxide is an inorganic compound with the formula CdO. It is one of the main precursors to other cadmium compounds. It crystallizes in a cubic rocksalt lattice like sodium chloride, with octahedral cation and anion centers. It occurs naturally as the rare mineral monteponite. Cadmium oxide can be found as a colorless amorphous powder or as brown or red crystals. Cadmium oxide is an n-type semiconductor with a band gap of 2.18 eV at room temperature.
Electroless nickel-phosphorus plating is a chemical process that deposits an even layer of nickel-phosphorus alloy on the surface of a solid substrate, like metal or plastic. The process involves dipping the substrate in a water solution containing nickel salt and a phosphorus-containing reducing agent, usually a hypophosphite salt. It is the most common version of electroless nickel plating and is often referred by that name. A similar process uses a borohydride reducing agent, yielding a nickel-boron coating instead.
Fluoroboric acid or tetrafluoroboric acid (archaically, fluoboric acid) is an inorganic compound with the chemical formula [H+][BF4−], where H+ represents the solvated proton. The solvent can be any suitably Lewis-basic entity. For instance, in water, it can be represented by H
3OBF
4 (oxonium tetrafluoroborate), although more realistically, several water molecules solvate the proton: [H(H2O)n+][BF4−]. The ethyl ether solvate is also commercially available: [H(Et2O)n+][BF4−], where n is most likely 2. Unlike other strong acids like H2SO4 or HClO4, the pure unsolvated substance does not exist (see below).
Dihydrogen complexes are coordination complexes containing intact H2 as a ligand. They are a subset of sigma complexes. The prototypical complex is W(CO)3(PCy3)2(H2). This class of compounds represent intermediates in metal-catalyzed reactions involving hydrogen. Hundreds of dihydrogen complexes have been reported. Most examples are cationic transition metals complexes with octahedral geometry.
Transition metal hydrides are chemical compounds containing a transition metal bonded to hydrogen. Most transition metals form hydride complexes and some are significant in various catalytic and synthetic reactions. The term "hydride" is used loosely: some of them are acidic (e.g., H2Fe(CO)4), whereas some others are hydridic, having H−-like character (e.g., ZnH2).
Cadmium cyanide is an inorganic compound with the formula Cd(CN)2. It is a white crystalline compound that is used in electroplating. It is very toxic, along with other cadmium and cyanide compounds.
Chemical Bath Deposition, also called Chemical Solution Deposition and CBD, is a method of thin-film deposition, using an aqueous precursor solution. Chemical Bath Deposition typically forms films using heterogeneous nucleation, to form homogeneous thin films of metal chalcogenides and many less common ionic compounds. Chemical Bath Deposition produces films reliably, using a simple process with little infrastructure, at low temperature (<100˚C), and at low cost. Furthermore, Chemical Bath Deposition can be employed for large-area batch processing or continuous deposition. Films produced by CBD are often used in semiconductors, photovoltaic cells, and supercapacitors, and there is increasing interest in using Chemical Bath Deposition to create nanomaterials.
Boron monofluoride or fluoroborylene is a chemical compound with formula BF, one atom of boron and one of fluorine. It was discovered as an unstable gas and only in 2009 found to be a stable ligand combining with transition metals, in the same way as carbon monoxide. It is a subhalide, containing fewer than the normal number of fluorine atoms, compared with boron trifluoride. It can also be called a borylene, as it contains boron with two unshared electrons. BF is isoelectronic with carbon monoxide and dinitrogen; each molecule has 14 electrons.
Nickel compounds are chemical compounds containing the element nickel which is a member of the group 10 of the periodic table. Most compounds in the group have an oxidation state of +2. Nickel is classified as a transition metal with nickel(II) having much chemical behaviour in common with iron(II) and cobalt(II). Many salts of nickel(II) are isomorphous with salts of magnesium due to the ionic radii of the cations being almost the same. Nickel forms many coordination complexes. Nickel tetracarbonyl was the first pure metal carbonyl produced, and is unusual in its volatility. Metalloproteins containing nickel are found in biological systems.
Transition metal nitrile complexes are coordination compounds containing nitrile ligands. Because nitriles are weakly basic, the nitrile ligands in these complexes are often labile.
{{cite journal}}
: Cite journal requires |journal=
(help)