Tetrakis(dimethylamino)zirconium

Base Information

• Chemical Name: Tetrakis(dimethylamino)zirconium
• CAS No.: 19756-04-8
• Molecular Formula: C8H24N4Zr
• Molecular Weight: 267.529
• Hs Code.: 29310099
• European Community (EC) Number: 629-068-5
• Mol file: 19756-04-8.mol

Synonyms:TETRAKIS(DIMETHYLAMINO)ZIRCONIUM;19756-04-8;TDMAZ;Zirconium, tetrakis(dimethylamino)-;Tetrakis(dimethylamido)zirconium(IV);17828-33-0;Tetrakis(dimethylamino)zirconium(IV);dimethylazanide;zirconium(4+);TDMAZ: Zr[N(CH3)2]4;MFCD00239502;Zr(NMe2)4;SCHEMBL77142;CS-0099001;Tetrakis(dimethylamido)zirconium(IV), crystalline;Tetrakis(dimethylamido)zirconium(IV), deposition grade;Tetrakis(dimethylamido)zirconium(IV), packaged for use in deposition systems;Tetrakis(dimethylamido)zirconium(IV), electronic grade, >=99.99% trace metals basis;Tetrakis(dimethylamino)zirconium(IV), 99% (99.99%-Zr) TDMAZ, contained in 50ml Swagelok? cylinder for CVD/ALD

Chemical Property of Tetrakis(dimethylamino)zirconium

Chemical Property:

• Appearance/Colour: Pale yellow-greenish crystalline solid
• Melting Point: 57-60 °C(lit.)
• Boiling Point: 80°C 0,1mm
• Flash Point: >65℃
• PSA: 12.96000
• LogP: 0.04920
• Storage Temp.: water-free area
• Sensitive.: moisture sensitive, store cold
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 266.104796
• Heavy Atom Count: 13
• Complexity: 24.1

Purity/Quality:

99.0% ^*data from raw suppliers

Tetrakis(dimethylamino)zirconium, 99% TDMAZ ^*data from reagent suppliers

Safty Information:

• Pictogram(s): F,Xi
• Hazard Codes: F,Xi
• Statements: 11-14/15-36/37/38
• Safety Statements: 16-26-36-43

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C[N-]C.C[N-]C.C[N-]C.C[N-]C.[Zr+4]
• General Description: **Null** (The provided abstract does not contain relevant information about the properties, synthesis, or applications of **TETRAKIS(DIMETHYLAMINO)ZIRCONIUM**; it primarily discusses borane ligands and their titanium/zirconium complexes.)

Technology Process of Tetrakis(dimethylamino)zirconium

There total 14 articles about Tetrakis(dimethylamino)zirconium which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

zirconium(IV) chloride (10026-11-6) + dimethyl amine (124-40-3) → tetrakis(dimethylamido)zirconium (IV) (19756-04-8)

Guidance literature:

dimethyl amine; With n-butyllithium; In hexane; at -10 - 20 ℃; for 4h;

zirconium(IV) chloride; In hexane; at 0 - 20 ℃; for 4h; Time;

Reference yield: 86.0%

2Li(1+)*6C2H6N(1-)*Zr(4+)*2C4H8O + zirconium(IV) chloride (10026-11-6) → tetrakis(dimethylamido)zirconium (19756-04-8)

Guidance literature:

In benzene; at 20 ℃; for 0.166667h; Inert atmosphere;

DOI:10.1021/acscatal.5b01671

Reference yield: 83.0%

lithium dimethylamide (3585-33-9) + zirconium(IV) chloride (10026-11-6) → tetrakis(dimethylamido)zirconium (IV) (19756-04-8)

Guidance literature:

In toluene; N2-atmosphere; stirring (room temp., 18 h); evapn. (reduced pressure), subliming (80°C, 0.05 mmHg);

DOI:10.1021/om00001a003

upstream raw materials:

lithium dimethylamide

Zr(NMe₂)3(Si(SiMe₃)3)

water

zirconium(IV) chloride

Downstream raw materials:

zirconium(IV) oxide

Zr(N(CH₃)2)3(OC₄H₈)2⁽¹⁺⁾*B(C₆H₅)4^(1-)=[Zr(N(CH₃)2)3(OC₄H₈)2]B(C₆H₅)4

[Zr(N(CH₃)2)2(C₁₀H₆(NC₆H₅)C₉H₆N)2]

[Zr(C₁₀H₆(N(benzyl))C₉H₆N)(NMe₂)3]

Refernces

Synthesis of cyclopentadienyl-, indenyl-, and fluorenylbis(pentafluorophenyl)boranes as ligands in titanium and zirconium half-sand wich complexes. The crystal structures of C₁₃H₉B(C₆F₅) ₂·t-BuNH₂, C₁₃H₈SiMe₃B(C₆F₅) ₂, and {η⁵-C₅H

10.1021/om970433j

The research focuses on the synthesis and study of various borane compounds and their complexes with titanium and zirconium. Key chemicals involved include bis(pentafluorophenyl)boron fluoride (C6F5)2BF?OEt2, which is used as a precursor to synthesize fluorenylborane (Flu)B(C6F5)2 and indenylboranes 1- and 2-IndB(C6F5)2. These boranes are further reacted with various metal compounds such as Zr(NMe2)4 and TiCl4 to form half-sandwich complexes like {C5H4B(C6F5)2}TiCl3. The study also explores the formation of adducts with tert-butylamine and investigates the catalytic activity of these complexes in ethene polymerization. The crystal structures of several compounds, including (Flu)B(C6F5)2?NH2CMe3, Flu(SiMe3)B(C6F5)2, and {C5H4B(C6F5)2}TiCl3, are determined by X-ray diffraction, providing insights into their molecular structures and bonding characteristics.