IP Library Granted Patent US 7,964,722
Granted Patent B2
US 7,964,722 · App. 10/874,356 · Granted Jun 21, 2011

Light-driven rotary molecular motors

Assignee: Board of Regents of the Nevada System of Higher Education, on behalf of the University of Nevada, Reno
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 7,964,722
App. No.
10/874,356
Granted
Jun 21, 2011
Kind
B2
Abstract

Compounds of Formula (1) are disclosed. C b is a carbocyclic or heterocyclic group having an atom within the cyclic structure selected from C, N, Si, and C r and singly bound to A. A is CR, COR, CSR, CNR 2 , CCN, CCONR 2 , CNO 2 , CNNAr, CX 1 , or N. C r is a chromophore having a substantially planar cyclic structure. The compounds function as nanometer-scale rotary molecular motors powered and controlled by light energy. The design of the molecular motor devices is flexible so that the rotary direction, drive light wavelength, and other physical characteristics can be varied. The compounds can be chemically functionalized to allow it to be integrated into or attached to a variety of structures. The device can be used in applications where mechanical power, positional control, and information encoding are to be generated at the size scale of individual molecules.

Claims (89)

1. A compound of formula (2):

wherein:

C b is a carbocyclic or heterocyclic group wherein the atom within the cyclic structure is singly bound to A and is a bridgehead carbon atom;

A is CR, COR, CSR, CNR 2 , CCN, CCONR 2 , CNO 2 , CNNAr, or CX′, wherein Ar is aryl or heteroaryl and X′ is a halide;

G is CR 2 , >C═CR 2 , C═O, C═S, C═NR, NR, O, or S;

n is 0, 1, or 2;

E is independently CH, CH 2 , N, NH, O, or S;

m is independently 0, 1, 2, or 3;

X is independently R 1 , SiR 1 3 , ═NR 1 , NR 1 2 , ═O, OR 1 , ═S, or SR 1 ;

Y is independently R 1 , SiR 1 3 , ═NR 1 , NR 1 2 , ═O, OR 1 , ═S, or SR 1 ;

q is independently 0, 1, 2, 3, or 4;

R is independently H;

substituted or unsubstituted, branched or straight chain C 1 -C 18 alkyl;

substituted or unsubstituted, branched or straight chain C 2 -C 18 alkenyl;

substituted or unsubstituted, branched or straight chain C 2 -C 18 alkynyl;

—(OCH 2 CH 2 ) 1-15 OH; —(OC 3 H 6 ) 1-15 OH;

substituted or unsubstituted, saturated or unsaturated, carbocycles or heterocycles; or

substituted or unsubstituted aryl or heteroaryl; and

R 1 is independently H;

substituted or unsubstituted, branched or straight chain C 1 -C 18 alkyl;

substituted or unsubstituted, branched or straight chain C 2 -C 18 alkenyl;

substituted or unsubstituted, branched or straight chain C 2 -C 18 alkynyl;

—(OCH 2 CH 2 ) 1-15 OH; —(OC 3 H 6 ) 1-15 OH;

substituted or unsubstituted, saturated or unsaturated, fused or unfused carbocycles or heterocycles; or

substituted or unsubstituted, fused or unfused aryl or heteroaryl;

wherein when R 1 is a cyclic structure the heteroatoms Si, N, O, or S within the definitions of X and Y may form part of the cyclic structure.

2. A compound of claim 1 , wherein C b is a bi-cyclic carbocycle or heterocycle.

3. A compound of claim 1 , wherein C b is a tri-cyclic carbocycle or heterocycle.

4. A compound of claim 1 , wherein

A is CR;

G is CR 2 , NR, O, or S;

n is 0 or 1;

E is independently CH, CH 2 , N, NH, O, or S;

m is independently 1 or 2;

X is independently R 1 , ═NR 1 , NR 1 2 , ═O, OR 1 , ═S, or SR 1 ;

Y is independently R 1 , ═NR 1 , NR 1 2 , ═O, OR 1 , ═S, or SR 1 ;

q is independently 0, 1, 2, 3, or 4;

R is independently H;

substituted or unsubstituted, branched or straight chain C 1 -C 9 alkyl;

substituted or unsubstituted, branched or straight chain C 2 -C 9 alkenyl;

substituted or unsubstituted, branched or straight chain C 2 -C 9 alkynyl;

—(OCH 2 CH 2 ) 1-7 OH; —(OC 3 H 6 ) 1-7 OH;

substituted or unsubstituted, saturated or unsaturated, carbocycles or heterocycles; or

substituted or unsubstituted aryl or heteroaryl; and

R 1 is independently H;

substituted or unsubstituted, branched or straight chain C 1 -C 9 alkyl;

substituted or unsubstituted, branched or straight chain C 2 -C 9 alkenyl;

substituted or unsubstituted, branched or straight chain C 2 -C 9 alkynyl;

—(OCH 2 CH 2 ) 1-7 OH; —(OC 3 H 6 ) 1-7 OH;

substituted or unsubstituted, saturated or unsaturated, fused or unfused carbocycles or heterocycles; or

substituted or unsubstituted, fused or unfused aryl or heteroaryl;

wherein when R 1 is a cyclic structure the heteroatoms Si, N, O, or S within the definitions of X and Y may form part of the cyclic structure.

5. A compound of claim 4 , wherein

A is CR;

G is CR 2 , or NR;

n is 0 or 1;

E is independently CH, CH 2 , N, or NH;

each m is 1;

X is independently R 1 , NR 1 2 , OR 1 , or SR 1 ;

Y is independently R 1 , NR 1 2 , or OR 1 ;

q is independently 0, 1, or 2;

R is independently H;

substituted or unsubstituted, branched or straight chain C 1 -C 5 alkyl;

substituted or unsubstituted, branched or straight chain C 2 -C 5 alkenyl;

substituted or unsubstituted, branched or straight chain C 2 -C 5 alkynyl;

substituted or unsubstituted, saturated or unsaturated, carbocycle or heterocycle selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, pyrrolidinyl, piperidyl, imidazolidinyl, pyrazolidinyl, pyrazolinyl, piperazinyl, morpholinyl, chromanyl, indolinyl, and their corresponding iso-forms; or

substituted or unsubstituted fused or unfused aryl or heteroaryl selected from the group consisting of phenyl, benzyl, naphthyl, furyl, benzofuranyl, pyranyl, pyrazinyl, thienyl, pyrrolyl, imidazolyl, pyridyl, pyrimidinyl, pyridazinyl, indolyl, indolizinyl, indoazolyl, purinyl, quinolyl, thiazolyl, phthalazinyl, quinoxalinyl, quinazolinyl, benzothienyl, anthryl, phenathtryl, and their corresponding iso-forms; and

R 1 is independently H;

substituted or unsubstituted, branched or straight chain C 1 -C 4 alkyl;

substituted or unsubstituted, branched or straight chain C 2 -C 4 alkenyl;

substituted or unsubstituted, branched or straight chain C 2 -C 4 alkynyl;

substituted or unsubstituted, saturated or unsaturated, fused or unfused carbocycles or heterocycles selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, pyrrolidinyl, piperidyl, imidazolidinyl, pyrazolidinyl, pyrazolinyl, piperazinyl, morpholinyl, chromanyl, indolinyl, and their corresponding iso-forms; or

substituted or unsubstituted fused or unfused aryl or heteroaryl selected from the group consisting of phenyl, benzyl, naphthyl, furyl, benzofuranyl, pyranyl, pyrazinyl, thienyl, pyrrolyl, imidazolyl, pyridyl, pyrimidinyl, pyridazinyl, indolyl, indolizinyl, indoazolyl, purinyl, quinolyl, thiazolyl, phthalazinyl, quinoxalinyl, quinazolinyl, benzothienyl, anthryl, phenathtryl, and their corresponding iso-forms.

6. A compound of claim 5 , wherein

A is CR;

G is CR 2 , or NR;

n is 0 or 1;

E is independently CH, CH 2 , N, or NH;

each m is 1;

X is independently R 1 , NR 1 2 , or OR 1 ;

Y is independently R 1 , NR 1 2 , or OR 1 ;

q is independently 0, 1, or 2;

R is independently H, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, cyclopentyl, cyclohexyl, phenyl, or pyridinyl; and

R 1 is independently H, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, cyclopentyl, cyclohexyl, phenyl, or pyridinyl.

7. A compound of claim 1 , wherein the moiety of formula (2) defined by

is selected from the group consisting of 4H-cyclopenta-[def]phenanthrene, 7H-dibenzo[c,g]fluorene, 13H-dibenzo[a,i]fluorene, 13H-dibenzo[a,g]fluorene, 11H-benzo[a]fluorene, 7H-benzo[c]fluorene, and derivatives of hexafulvenes and heptafulvenes.

8. A compound of formula (2) as recited in claim 1 having the structure:

wherein Z is substituted or unsubstituted, branched or straight chain C 3 -C 9 alkylene; substituted or unsubstituted, branched or straight chain C 3 -C 9 alkenylene; substituted or unsubstituted, branched or straight chain C 3 -C 9 alkynylene; —(OCH 2 CH 2 ) 1-3 O—; —(OC 3 H 6 ) 1-3 O—; substituted or unsubstituted, saturated or unsaturated, divalent carbocycles or heterocycles; or substituted or unsubstituted arylene or heteroarylene.

9. A compound of formula (2) as recited in claim 1 having the structure:

Assignments (4)
CONFIRMATORY LICENSE Recorded Jul 11, 2012
From: UNIVERSITY OF NEVADA RENO
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 028546/0345 →
CHANGE OF NAME Recorded Jun 30, 2010
From: BOARD OF REGENTS OF THE UNIVERSITY AND COMMUNITY COLLEGE SYSTEM OF NEVADA ON BEHALF OF THE UNIVERSITY OF NEVADA, RENO
To: BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION, ON BEHALF OF THE UNIVERSITY OF NEVADA, RENO
Reel/Frame 024616/0375 →
CONFIRMATORY LICENSE Recorded Oct 25, 2006
From: UNIVERSITY OF NEVADA RENO
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 018432/0170 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2005
From: BELL, THOMAS W.; CLINE, JOSEPH L.; CREMO, CHRISTINE R.; GILLETT, STEPHEN L.; FREDERICK, JOHN H.
To: BOARD OF REGENTS OF THE UNIVERSITY AND COMMUNITY COLLEGE SYSTEM OF NEVADA ON BEHALF OF THE UNIVERSITY OF NEVADA OF RENO, THE
Reel/Frame 016394/0262 →
Continuity (1)
Related Publication 20110077394A1 · Mar 31, 2011