Related Experiment Video
Updated: Jan 18, 2026

Synthesis of In37P20O2CR51 Clusters and Their Conversion to InP Quantum Dots
Published on: May 7, 2019
A Crystalline Mono-Coordinate Indium(I)-Phosphaalkenyl
Álvaro García-Romero1, Maren Pink1, Israel Fernández2
1Department of Chemistry, Indiana University, 800 East Kirkwood Ave., Bloomington, Indiana, 47405, USA.
Abstract:
The synthesis of the mono-coordinate indium(I) compound In[C(Ad)═PTer] (Ad = 1-adamantyl, Ter = 2,6-Dipp2-C6H3; Dipp = 2,6-diisopropylphenyl) is reported. Key to the formation of this monomeric species is the steric protection offered by the supporting phosphaalkenyl ligand which hinders aggregation. The title compound can be accessed from the reaction of (InTer)2 with the phosphaalkyne AdC≡P in an unusual redox-neutral transformation in which the In─C bond of the (InTer)2 precursor, known to dissociate in solution, adds across the C≡P triple bond of the phosphaalkyne. This insertion reaction is reversible, as shown by the reaction of In[C(Ad)═PTer] with B(C6F5)3, which affords [TerInB(C6F5)3] accompanied by extrusion of AdC≡P. In contrast, the lighter analogue (GaTer)2 promotes the dimerization of the AdC≡P fragment resulting in the formation of the cluster (GaTer)2(AdCP)2. The formal oxidation state of In[C(Ad) = PTer] was probed by reaction with methyl-iodide which affords the indium(III) compound In(Me)I[C(Ad) = PTer] in a formal single-site oxidative-addition reaction at indium.
Related Concept Videos
Ionic Crystal Structures
Most monatomic ions behave as charged spheres, and their attraction for ions of opposite charge is the same in every direction. Consequently, stable structures for ionic compounds result (1) when ions of one charge are surrounded by as many ions as possible of the opposite...
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Metallic Solids
All metallic solids exhibit high thermal and electrical conductivity, metallic luster, and malleability....
Structural Isomerism
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Stereoisomerism
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...

