IP Library Granted Patent US 10,562,920
Granted Patent B2
US 10,562,920 · App. 15/566,058 · Granted Feb 18, 2020

Ln(III) and Ga(III) metallacrown complexes

Inventors: Evan R. Trivedi (Ann Arbor, MI); Vincent L. Pecoraro (Ann Arbor, MI); Svetlana V. Eliseeva (Orléans, FR); Stépane Petoud (Orléans, FR); Chun Y. Chow (Ann Arbor, MI); Tu Ngoc Nguyen (Ann Arbor, MI); Jacob Charles Lutter (Ypsilanti, MI); Ivana Martinic (Orléans, FR)
Assignees: THE REGENTS OF THE UNIVERSITY OF MICHIGAN; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE
C07F5/00C07F5/003C07F19/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,562,920
App. No.
15/566,058
Granted
Feb 18, 2020
Kind
B2
Abstract

The present invention concerns heterometallic metallacrown compounds incorporating Ga(III) and Ln(III) cations, with a templating ligand such as salicylhydroxamic acid or derivatives thereof, wherein said metallacrown contains at least one repeating [—Ga—N—O—] sub-unit where the N—O derives from the templating ligand.

Claims (13)

1. A heterometallic metallacrown compound incorporating Ga(III) and Ln(III) cations, with a templating ligand being isophthalic acid, salicylic hydroxamic acid or derivatives thereof, wherein said metallacrown contains at least one repeating [—Ga—N—O—] sub-unit where the N—O derives from the templating ligand.

2. The heterometallic metallacrown compound of claim 1 , including a Ln(III)[12-MC Ga III N(shi) -4] core, wherein MC Ga III N(shi) is a metallacrown macrocycle with a repeating sub-unit consisting of Ga(III) ion and a salicylic hydroxamic acid (H 3 shi) ligand or its derivatives.

3. The heterometallic metallacrown compound of any one of claims 1 to 2 , including at least one countercation (C + ) which balances the charge of the compound.

4. The heterometallic metallacrown compound of claim 1 , having the formula: Ln(III)(OX) 4 [12-MC Ga III N(shi) -4](C + ), wherein MC Ga III N(shi) is a metallacrown macrocycle with a repeating sub-unit consisting of Ga(III) ion and a salicylic hydroxamic acid (H 3 shi) ligand or its derivatives, OX − are bridging carboxylate units and C+ are countercations that balance the charge of the compound.

5. The heterometallic metallacrown compound of claim 1 , having the formula: Ln 2 (isophthalate) 4 [12-MC GaNshi -4] 2 .

6. The heterometallic metallacrown compound of claim 1 , having the formula: Ln 3+ [12-MC Ga III N(shi) -4].

7. The heterometallic metallacrown compound of claim 1 , having the formula: Ga 6 Ln(shi) 9 .

8. The heterometallic metallacrown compound of claim 1 , wherein Ln(III) is chosen from the lanthanide ions consisting of: yttrium (Y 3+ ), lanthanum (La 3+ ), cerium (Ce 3+ ), praseodymium (Pr 3+ ), neodymium (Nd 3+ ), promethium (Pm 3+ ), samarium (Sm 3+ ), europium (Eu 3+ ), gadolinium (Gd 3+ ), terbium (Tb 3+ ), dysprosium (Dy 3+ ), holmium (Ho 3+ ), erbium (Er 3+ ), thulium (Tm 3+ ), ytterbium (Yb 3+ ), and lutetium (Lu 3+ ).

9. A method for bioanalytical assay or biological imaging, comprising contacting cells with the heterometallic metallacrown compound of claim 1 .

10. The heterometallic metallacrown compound of claim 1 , wherein the derivatives of salicylic hydroxamic acid have the following formula:

with any combination of R-groups bound at each of positions 3 through 6, each R-group being independently selected from the group consisting of —H, -D, —OH, —SH, —NH 2 , —NO 2 , —F, —Cl, —Br, —I, —CF 3 , —OCH 3 , —SO 3 H, —CH 3 , —CN, a fused aromatic ring, a fused heterocyclic ring, an amide, ═O, ═N, —N 3 , —NR′H, —NR′2, —NR′ 3+ , —COOH, —COOR′, —CH 2 —R′, —CHR 2 , —CHR′R″, —CR′R″R′″, —OR′, and combinations thereof, wherein R′, R″, and R′″ are independently selected from the group consisting of —H, -D, a fused aromatic ring, and a fused heterocyclic ring.

11. The heterometallic metallacrown compound of claim 1 , wherein the derivatives of isophthalic acid have the following formula:

with any combination of R-groups bound at each of positions 2, and 4 through 6, each R-group being independently selected from the group consisting of —H, -D, —OH, —SH, —NH 2 , —NO 2 , —F, —Cl, —Br, —I, —CF 3 , —OCH 3 , —SO 3 H, —CH 3 , —CN, a fused aromatic ring, a fused heterocyclic ring, an amide, ═O, ═N, —N 3 , —NR′H, —NR′2, —NR′ 3+ , —COOH, —COOR′, —CH 2 —R′, —CHR 2 , —CHR′R″, —CR′R″R′″, —OR′, and combinations thereof, wherein R′, R″, and R′″ are independently selected from the group consisting of —H, -D, a fused aromatic ring, and a fused heterocyclic ring.

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 20, 2019
From: UNIVERSITY OF MICHIGAN
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 048382/0966 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2018
From: TRIVEDI, EVAN R.; PECORARO, VINCENT L.; ELISEEVA, SVETLANA V.; PETOUD, STÉPHANE; CHOW, CHUN Y.; NGUYEN, TU NGOC; MARTINIC, IVANA; LUTTER, JACOB CHARLES
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE
Reel/Frame 047663/0817 →
Continuity (2)
Provisional Application 62149047 · Apr 17, 2015
Related Publication 20180127438A1 · May 10, 2018