The study of main-group molecules that behave and react similarly to transition-metal (TM) complexes has attracted significant interest in recent decades. Most notably, the attractive idea of replacing the all-too-often rare and costly metals from catalysis has motivated efforts to develop main-group-element-mediated reactions. Main-group elements, however, lack the electronic flexibility of TM complexes that arises from combinations of empty and filled d orbitals and that seem ideally suited to bind and activate many substrates. In this review, we look at boron, an element that despite its nonmetal nature, low atomic weight, and relative redox staticity has achieved great milestones in terms of TM-like reactivity. We show how in interelement cooperative systems, diboron molecules, and hypovalent complexes the fifth element can acquire a truly metallomimetic character. As we discuss, this character is powerfully demonstrated by the reactivity of boron-based molecules with H, CO, alkynes, alkenes and even with N.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.chemrev.8b00561DOI Listing

Publication Analysis

Top Keywords

metallomimetic chemistry
4
chemistry boron
4
boron study
4
study main-group
4
main-group molecules
4
molecules behave
4
behave react
4
react transition-metal
4
transition-metal complexes
4
complexes attracted
4

Similar Publications

While existing literature has primarily focused on carbene-stabilized amino- and arylborylenes of the form [(carbene)BR] (R = substituent), herein we report the generation and metallomimetic reactivity of the first carbene-stabilized alkylborylene [(CAACMe)BCy] (CAACMe = 1-(2,6-diisopropylphenyl)-3,3,5,5-tetramethylpyrrolidin-2-ylidene, Cy = cyclohexyl. Furthermore, the transition metal-like decarbonylation reactions of a borylene complex, [(CAACMe)BCy(CO)], derived from borylene [(CAACMe)BCy] and CO, are described. Additional findings described include (i) the identification of the coordination stages of the ligand to boron towards forming complexes [(CAACMe)BCyL] in the reduction route from starting material [(CAACMe)BCyBr2] and in the photolysis route from carbonyl complex [(CAACMe)BCy(CO], and (ii) insights from quantum-chemical computations regarding the molecular and electronic structure of the borylene at various stages.

View Article and Find Full Text PDF

Electron-rich ditriflato- and dibromido-diborane(4) molecules with bridging guanidinate substituents readily eliminate triflate/bromide to give monocationic diboranes displaying a dual reactivity as Lewis acids and electron donors. In this work, we report unprecedented reaction sequences in which pyrazine derivatives are first coordinated to the diborane. These coordination compounds are intensely coloured due to electronic excitations from an electron in the B-B bond to a pyrazine π* orbital.

View Article and Find Full Text PDF

The dual reactivity of boron compounds as Lewis acids and electron donors has spurred the development of a metallomimetic chemistry of boron compounds as a topical research theme. In this work we elaborate on the reaction of specially-designed diborane(4) compounds with quinones, as a prime example showing their dual (metallomimetic) chemistry as a Lewis acid and electron donor. The quinone is first coordinated to the diborane and then reduced by intramolecular electron transfer from the B-B bond to a quinone π* orbital.

View Article and Find Full Text PDF

Synthesis and redox catalysis of Carbodiphosphorane ligated stannylene.

Nat Commun

November 2024

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, 610064, Chengdu, People's Republic of China.

Heavier group 14 carbene analogues, exhibiting transition-metal-like behavior, display remarkable capability for small molecule activation and coordination chemistry. However, their application in redox catalysis remains elusive. In this paper, we report the synthesis and isolation of a stannylene with carbodiphosphorane ligand.

View Article and Find Full Text PDF

Hydrogen splitting at a single phosphorus centre and its use for hydrogenation.

Nat Chem

August 2024

School of Chemistry, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv, Israel.

Catalytic processes are largely dominated by transition-metal complexes. Main-group compounds that can mimic the behaviour of the transition-metal complexes are of great interest due to their potential to substitute or complement transition metals in catalysis. While a few main-group molecular centres were shown to activate dihydrogen via the oxidative addition process, catalytic hydrogenation using these species has remained challenging.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!